Japanese macaque herpesvirus nucleic acid and polypeptide sequences and their use

ABSTRACT

Japanese macaques can harbor a virus related to RRV, called Japanese macaque herpesvirus (JMHV). An isolated virus is disclosed herein (Japanese macaque herpesvirus, JMHV) as deposited with ATCC as Deposit Accession No. PTA-1884, deposited May 18, 2000, as are viral particles including this virus and host cells infected with this virus. The entire nucleic acids sequence of this virus is provided herein. Also disclosed are the nucleic acid sequences of unique open reading frames, and the polypeptide sequences encoded by these open reading frames. Pharmaceutical compositions are also disclosed that include the viral nucleic acid, a polypeptide encoded by the viral nucleic acid, an antibody that binds the JMHV polypeptide, or a polynucleotide encoding at least one JMHV polypeptide. Model systems for screening for agents of use in the treatment of MS are also disclosed.

PRIORITY CLAIM

[0001] This is a continuation-in part of U.S. application Ser. No. 10/276,524, filed Nov. 13, 2002, which is a § 371 U.S. national stage of International Application No. PCT/US01/16274, filed May 17, 2001, which was published in English under PCT Article 21(2), and claims the benefit of U.S. Provisional Application No. 60/205,652 filed May 18, 2000. These applications are incorporated herein by reference.

STATEMENT OF GOVERNMENT SUPPORT

[0002] This disclosure was made with United States government support pursuant to grant RR00163 and CA75922 from the National Institutes of Health; the United States government has certain rights in the invention.

FIELD

[0003] This application relates to a Japanese macaque herpesvirus (JMHV), specifically to the nucleic acid sequence of the virus, open reading frames in this virus, and to amino acid sequences encoded by these sequences. Compositions and methods are provided for the production of animal models useful in assessing the efficacy of drugs for the treatment or prevention of conditions associated with infection by the virus, such as multiple sclerosis.

BACKGROUND

[0004] An autoimmune disease is a condition that results from a pathological immune reaction against an individual's own tissues. Examples of autoimmune diseases, in which the immune system attacks otherwise healthy tissue include multiple sclerosis (MS), autoimmune uveitis, myasthenia gravis (MG), psoriasis, and rheumatoid arthritis (RA).

[0005] Multiple sclerosis (MS) is a chronic, neurological, autoimmune, demyelinating disease. MS can cause blurred vision, unilateral vision loss (optic neuritis), loss of balance, poor coordination, slurred speech, tremors, numbness, extreme fatigue, changes in intellectual function (such as memory and concentration), muscular weakness, paresthesias, and blindness. Many subjects develop chronic progressive disabilities, but long periods of clinical stability may interrupt periods of deterioration. Neurological deficits may be permanent or evanescent. In the United States there are about 250,000 to 400,000 persons with MS, and every week about 200 new cases are diagnosed. Worldwide, MS may affect 2.5 million individuals. Because it is not contagious, which would require U.S. physicians to report new cases, and because symptoms can be difficult to detect, the incidence of disease is only estimated and the actual number of persons with MS could be much higher.

[0006] The pathology of MS is characterized by an abnormal immune response directed against the central nervous system. In particular, T-lymphocytes are activated against the myelin sheath of the central nervous system causing demyelination. In the demyelination process, myelin is destroyed and replaced by scars of hardened “sclerotic” tissue which is known as plaque. These lesions appear in scattered locations throughout the brain, optic nerve, and spinal cord. Demyelination interferes with conduction of nerve impulses, which produces the symptoms of multiple sclerosis. Most patients recover clinically from individual bouts of demyelination, producing the classic remitting and exacerbating course of the most common form of the disease known as relapsing-remitting multiple sclerosis.

[0007] Although the immune system plays an important role in the pathogenesis of MS, epidemiological data and the inflammatory nature of the disease suggests that a viral or bacterial infection may trigger the autoimmune attack against nerve cells in genetically susceptible individuals. Many pathogens have been associated with MS, such as Epstein-Barr virus (EBV), Herpes simplex virus type 1 (HSV-1), Human herpesvirus-6 (HHV-6) and Chlamydia pneumoniae. While there is no solid evidence that supports any one infectious agent as the causative agent of MS, experimental models suggest that the disease may result from one of three different mechanisms including: i) immunologic response against bacterial/viral antigens in the central nervous system (CNS), resulting in demyelination; ii) an infectious agent in CNS that releases myelin antigens that initiate an autoimmune reaction against myelin, a concept referred to as “epitope spread”; and iii) a virus or bacteria that contains antigens with significant homology with myelin antigens and thus elicit an immunologic response against the infectious agent and the myelin antigens, a process referred to as “molecular mimicry.”

[0008] There is a need to develop animal models of multiple sclerosis. Specifically, these animal models can be used to evaluate agents that can be used to treat this disease. Any treatment that could delay the progression or recurrence of the disease would be enormously beneficial to people who have this disease, by reducing neurological impairment and disability.

SUMMARY

[0009] Japanese macaques can harbor a virus related to Rhesus macaque rhadinovirus (RRV), called Japanese macaque herpesvirus (JMHV). An isolated virus is disclosed herein (Japanese macaque herpesvirus, JMHV) as deposited with ATCC as Deposit Accession No. PTA-1884, deposited May 18, 2000, as are viral particles including this virus and host cells infected with this virus. The entire nucleic acids sequence of this virus is provided herein. Also disclosed are the nucleic acid sequences of unique open reading frames, and the polypeptide sequences encoded by these open reading frames. Pharmaceutical compositions are also disclosed that include the viral nucleic acid, a polypeptide encoded by the viral nucleic acid, an antibody that binds the JMHV polypeptide, or a polynucleotide encoding at least one JMHV polypeptide.

[0010] In one embodiment, a method is provided for testing the efficacy of a drug in the treatment of a condition associated with infection with JMHV. In one example, the method includes administering the drug to a non-human primate infected with JMHV; and observing the non-human primate to determine if the drug prevents or reduces the presentation of one or more symptoms associated with JMHV infection.

[0011] In a further embodiment, a method is provided for detecting the presence of JMHV or a related virus in a biological specimen, by amplifying by polymerase chain reaction a JMHV nucleic acid sequence, or by using hybridization technology, if such sequence is present in the sample.

[0012] A method is also provided for detecting the presence of JMHV in a biological specimen, including contacting the biological specimen with an antibody that binds to a JMHV polypeptide, and detecting binding of the antibody to the biological specimen or a component thereof. Binding of the antibody to the biological specimen indicates the presence of JMHV.

[0013] Kits are provided that include an antibody that binds to a JMHV polypeptide or an oligonucleotide that hybridizes to a JMHV nucleic acid sequence.

[0014] The foregoing and other objects, features, and advantages of the disclosure will become more apparent from the following detailed description of several examples which proceeds with reference to the accompanying figures.

BRIEF DESCRIPTION OF THE FIGURES

[0015]FIG. 1 is a schematic diagram of an ORF map of the JMHV genome. Map of the JMHV genome showing the ORFs that are homologous to JMHV, RRV, Kaposi's sarcoma-associated herpesvirus (KSHV) and Herpesvirus saimiri (HVS) (light gray arrows), JMHV and RRV (gray arrows), JMHV, RRV and KSHV (white arrows), JMHV unknown (black arrows), and JMHV unique (dark gray arrows). JMHV putative genes are numbered according to Table 1 from JM1 to JM171.

SEQUENCE LISTING

[0016] The nucleic and amino acid sequences listed in the accompanying sequence listing are shown using standard letter abbreviations for nucleotide bases, and three letter code for amino acids, as defined in 37 C.F.R. 1.822. Only one strand of each nucleic acid sequence is shown, but the complementary strand is understood as included by any reference to the displayed strand. In the accompanying sequence listing:

[0017] SEQ ID NO: 1 is the nucleic acid sequences of JMHV.

[0018] SEQ ID NOs: 2-172 are the amino acid sequences of polypeptides encoded by JMHV.

DETAILED DESCRIPTION

[0019] I. Abbreviations

[0020] CPE: Cytopathic effects

[0021] EAE: Autoimmune encephalomyelitis

[0022] JME: Japanese macaque encephalomyelitis

[0023] JMHV: Japanese macaque herpesvirus

[0024] MS: Multiple sclerosis

[0025] ORF: Open reading frame

[0026] PCR: Polymerase chain reaction

[0027] RRV: Rhesus macaque rhadinovirus

[0028] TEM: Transmission electron microscopy

[0029] II. Terms

[0030] Unless otherwise noted, technical terms are used according to conventional usage. Definitions of common terms in molecular biology may be found in Benjamin Lewin, Genes V, published by Oxford University Press, 1994 (ISBN 0-19-854287-9); Kendrew et al. (eds.), The Encyclopedia of Molecular Biology, published by Blackwell Science Ltd., 1994 (ISBN 0-632-02182-9); and Robert A. Meyers (ed.), Molecular Biology and Biotechnology: a Comprehensive Desk Reference, published by VCH Publishers, Inc., 1995 (ISBN 1-56081-569-8).

[0031] In order to facilitate review of the various embodiments of this disclosure, the following explanations of specific terms are provided.

[0032] Amplification of a nucleic acid molecule (for example, a DNA or RNA molecule): A technique that increases the number of copies of a nucleic acid molecule in a specimen. An example of amplification is the polymerase chain reaction in which a biological sample collected from a subject is contacted with a pair of oligonucleotide primers, under conditions that allow for the hybridization of the primers to a nucleic acid template in the sample. The primers are extended under suitable conditions, dissociated from the template, and then re-annealed, extended, and dissociated to amplify the number of copies of the nucleic acid. The product of amplification may be characterized by electrophoresis, restriction endonuclease cleavage patterns, oligonucleotide hybridization or ligation, and/or nucleic acid sequencing using standard techniques. Other examples of amplification include strand displacement amplification, as disclosed in U.S. Pat. No. 5,744,311; transcription-free isothermal amplification, as disclosed in U.S. Pat. No. 6,033,881; repair chain reaction amplification, as disclosed in WO 90/01069; ligase chain reaction amplification, as disclosed in EP 0320308; gap filling ligase chain reaction amplification, as disclosed in U.S. Pat. No. 5,427,930; and NASBA™ RNA transcription-free amplification, as disclosed in U.S. Pat. No. 6,025,134.

[0033] Animal: Living multicellular vertebrate organisms, a category which includes, for example, humans, non-human primates, mammals, and birds.

[0034] Antibody: Immunoglobulin molecules and immunologically active portions of immunoglobulin molecules, for instance, molecules that contain an antigen binding site that specifically binds (immunoreacts with) an antigen.

[0035] A naturally occurring antibody (for example, IgG, IgM, IgD) includes four polypeptide chains, two heavy (H) chains and two light (L) chains inter-connected by disulfide bonds. However, it has been shown that the antigen-binding function of an antibody can be performed by fragments of a naturally occurring antibody. Thus, these antigen-binding fragments are also intended to be designated by the term “antibody.” Specific, non-limiting examples of binding fragments encompassed within the term antibody include (i) an Fab fragment consisting of the V_(L), V_(H), CL, and CH1 domains; (ii) an Fd fragment consisting of the V_(H) and CH1 domains; (iii) an Fv fragment consisting of the V_(L) and V_(H) domains of a single arm of an antibody, (iv) a dAb fragment (Ward et al., Nature 341:544-546, 1989) which consists of a V_(H) domain; (v) an isolated complimentarity determining region (CDR); and (vi) an F(ab′)₂ fragment, a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region.

[0036] Immunoglobulins and certain variants thereof are known and many have been prepared in recombinant cell culture (for example, see U.S. Pat. No. 4,745,055; U.S. Pat. No. 4,444,487; WO 88/03565; EP 0256654; EP 0120694; EP 0125023; Faoulkner et al., Nature 298:286, 1982; Morrison, J. Immunol. 123:793, 1979; Morrison et al., Ann Rev. Immunol 2:239, 1984).

[0037] Autoimmune disorder: A disorder in which the immune system produces an immune response (e.g. a B cell or a T cell response) against an endogenous antigen, with consequent injury to tissues.

[0038] Cell: A plant, animal, insect, bacterial, or fungal cell.

[0039] Conservative variants: “Conservative” amino acid substitutions are those substitutions that do not substantially affect or decrease an activity or antigenicity of a JMHV polypeptide. Specific, non-limiting examples of a conservative substitution include the following examples: Original Conservative Residue Substitutions Ala Ser Arg Lys Asn Gln, His Asp Glu Cys Ser Gln Asn Glu Asp His Asn; Gln Ile Leu, Val Leu Ile; Val Lys Arg; Gln; Glu Met Leu; Ile Phe Met; Leu; Tyr Ser Thr Thr Ser Trp Tyr Tyr Trp; Phe Val Ile; Leu

[0040] The term conservative variation also includes the use of a substituted amino acid in place of an unsubstituted parent amino acid, provided that antibodies raised to the substituted polypeptide also immunoreact with the unsubstituted polypeptide. Non-conservative substitutions are those that reduce an activity or antigenicity.

[0041] Degenerate variant: A polynucleotide encoding a JMHV polypeptide that includes a sequence that is degenerate as a result of the genetic code. There are 20 natural amino acids, most of which are specified by more than one codon. Therefore, all degenerate nucleotide sequences are included in the disclosure as long as the amino acid sequence of the JMHV polypeptide encoded by the nucleotide sequence is unchanged.

[0042] Expression Control Sequences: Nucleic acid sequences that control and regulate the expression of a nucleic acid sequence, such as a heterologous nucleic acid sequence, to which it is operably linked. Expression control sequences are operably linked to a nucleic acid sequence when the expression control sequences control and regulate the transcription and, as appropriate, translation of the nucleic acid sequence. Thus expression control sequences can include appropriate promoters, enhancers, transcription terminators, polyA signals, a start codon (for instance, ATG) in front of a protein-encoding polynucleotide sequence, splicing signal for introns, maintenance of the correct reading frame of that gene to permit proper translation of mRNA, and stop codons. The term “control sequences” is intended to include, at a minimum, components whose presence can influence expression, and can also include additional components whose presence is advantageous, for example, leader sequences and fusion partner sequences. Expression control sequences can include a promoter.

[0043] A promoter is a minimal sequence sufficient to direct transcription of a nucleic acid. Promoters may be cell-type specific or tissue specific. A promoter includes necessary nucleic acid sequences near the start site of transcription, such as, in the case of a polymerase II type promoter, a TATA element. A promoter also optionally includes distal enhancer or repressor elements which can be located as much as several thousand base pairs from the start site of transcription. Both constitutive and inducible promoters are included (see for example, Bitter et al., Methods in Enzymology 153:516-544, 1987).

[0044] For example, when cloning in bacterial systems, inducible promoters such as pL of bacteriophage lambda, plac, ptrp, ptac (ptrp-lac-hybrid promoter) and the like may be used. In one embodiment, when cloning in mammalian cell systems, promoters derived from the genome of mammalian cells (for example, metallothionein promoter) or from mammalian viruses (for example, the retrovirus long terminal repeat; the adenovirus late promoter; the vaccinia virus 7.5K promoter) can be used. Promoters produced by recombinant DNA or synthetic techniques may also be used to provide for transcription of the nucleic acid sequences. A polynucleotide can be inserted into an expression vector that contains a promoter sequence which facilitates the efficient transcription of the inserted genetic sequence of the host. The expression vector typically contains an origin of replication, a promoter, as well as specific nucleic acid sequences that allow phenotypic selection of the transformed cells. In one embodiment, the promoter is a cytomegalovirus promoter.

[0045] Herpesvirus: Viruses that include large (genomes up to 235 kbp DNA) that are generally complex viruses such that the virus encodes about 35 virion proteins. Herpesviruses encode a variety of enzymes involved in nucleic acid metabolism, DNA synthesis and protein processing (protein kinase).

[0046] The herpesvirus particle is complex, and includes a core that has a toroidal shape, with the large DNA genome would around a proteinaceous core. The complex capsid surrounds the core. Outside the capsid is the tegument, a protein-filled region which appears amorphous in electron micrographs. On the outside of the particle is the envelope, which contains numerous glycoproteins.

[0047] Herpesvirus genomes can have a unique long (UL) and a unique short (US) region, bounded by inverted repeats. The repeats allow rearrangements of the unique regions and Herpesvirus genomes exist as a mixture of four isomers. Herpesvirus genomes also contain multiple repeated sequences. The JMHV genome, however, has a unique long region bound by inverted repeat, which is consistent for gamma-herpesvirues.

[0048] Homologs: Two nucleotide or amino acid sequences that share a common ancestral sequence and diverged when a species carrying that ancestral sequence split into two species. Homologs frequently show a substantial degree of sequence identity.

[0049] Immuno-compromised: Lacking a normal immune response. Immuno-compromised refers to a condition in which some or all of an animal's immune system is inoperative, leaving the animal with an increased susceptibility to infection or disease. An animal may be rendered immuno-compromised by a biological agent such as, in the case of non-human primates, Simian Immunodeficiency Virus (SIV). Many strains of SIV have been isolated and characterized; any SIV strain that produces an immuno-compromised state can be used in the present disclosure including, but not limited to, for example, SIVmac239 (Kestler et al., Science 248:1109-12, 1990), SIVmac251 (Daniels et al., Science 228:1201-4, 1985), SIVdeltaB670 (Murphy-Corb et al., Nature 321:435, 1986) and SIVmne (Benveniste et al., J. Virol. 62:2091-101, 1988). In addition, hybrid SIV/HIV chimeras as known in the field can be employed, as can HIV-2. Simian type D retroviruses (SRVs), which cause an AIDS-like disease in rhesus monkeys, can alternatively be used to immuno-compromise the animals in place of SIV. These viral agents are administered to the animal using conventional means, such as intravenous or intramuscular injection, or oral, intrarectal or intravaginal inoculation (also see Example 24). Either intact viral particles or viral DNA may be administered. As known in the field, plasmid constructs containing the entire SIV genome are infectious when inoculated into animals and so may be employed in place of purified viral DNA.

[0050] Alternatively, an animal may be rendered immuno-compromised by administration of agents that target the immune system, including but not limited to anti-CD3 antibody (CD3 being the T cell receptor) either alone or conjugated with a toxic moiety, or immunosuppressive compounds including prednisone, azathioprine, cyclosporine A, and cyclophosphamide. Where an immunosuppressive compound such as cyclosporine is employed, an allogenic stimulus (such as a blood transfusion) may be administered with the subsequent administration of RRV to activate infection.

[0051] Alternatively, other methods of rendering an animal immuno-compromised may be used, including radiation treatment and surgical intervention.

[0052] Immune response: A response of a cell of the immune system, such as a B cell, T cell, or monocyte, to a stimulus. In one embodiment, the response is specific for a particular antigen (an “antigen-specific response”). The response can also be a non-specific response (not targeted specifically to salivary polypeptides) such as production of lymphokines. In one embodiment, an immune response is a T cell response, such as a CD4+ response or a CD8+ response. In another embodiment, the response is a Th1 (a subset of helper T cells) response. In yet another embodiment, the response is a B cell response, and results in the production of specific antibodies.

[0053] Isolated: An “isolated” biological component (such as a nucleic acid, peptide or protein) has been substantially separated, produced apart from, or purified away from other biological components in the cell of the organism in which the component naturally occurs, i.e., other chromosomal and extrachromosomal DNA and RNA, and proteins. Nucleic acids, peptides and proteins which have been “isolated” thus include nucleic acids and proteins purified by standard purification methods. The term also embraces nucleic acids, peptides and proteins prepared by recombinant expression in a host cell as well as chemically synthesized nucleic acids.

[0054] Japanese Macaque Herpesvirus (JMHV): A virus having the virological, immunological or pathological characteristics of Japanese macaque herpesvirus (e.g. JMHV 17792). JMHV causes the symptoms of MS in Japanese macaque monkeys which are infected with the virus. In particular examples, the JMHV has at least 85% (for example at least 90%, 95% or 98%) sequence identity to the JMHV deposited with the virus deposited as ATCC Accession No. PTA-1884. In other examples, the JMHV has at least 90%, 91%, 92%, 93%, 94%, 95%, or 98% homology with an RRV (e.g. ATCC VR-2901). Without being bound by theory, the JMHV may be derived from an RRV (see the experimental examples).

[0055] JMHV 17792: Japanese macaque herpesvirus isolate 17792. A Budapest Treaty deposit of JMHV 17792 was made with the American Type Culture Collection (ATCC), Manassas, Va., on May 18, 2001. This virus may be grown on primary Japanese macaque fibroblasts, using standard virological techniques. Alternatively, it may be grown on commercially available macaque cell lines. Infection of a non-human primate with JMHV 17792 can be accomplished using any standard method, including intravenous injection. In one embodiment, infection is achieved using 106 plaque forming units of JMHV 17792.

[0056] Label: A detectable compound or composition that is conjugated directly or indirectly to another molecule to facilitate detection of that molecule. Specific, non-limiting examples of labels include fluorescent tags, enzymatic linkages, and radioactive isotopes.

[0057] Multiple Sclerosis: A chronic, progressive disease of the central nervous system. Currently, the exact cause of the disease is unknown and there is no cure. Multiple sclerosis refers to multiple areas of patchy scarring, or plaques, that result from demyelination (destruction of myelin, a fatty insulation covering the nerve fibers). When the myelin sheath is destroyed during the MS disease process, signals transmitted throughout the CNS are slowed or disrupted. In many cases, the body may compensate for the loss of myelin by increasing the density of the sodium channels so that action potentials can continue to be carried, in spite of loss of myelin. The nerves also retain the capacity to remyelinate. Unfortunately, the disease process often outpaces these corrective actions.

[0058] The symptoms, severity, and course of MS vary widely depending partly on the sites of the plaques and the extent of the demyelination. Experts generally group multiple sclerosis into four types: relapsing-remitting, primary-progressive, secondary-progressive, and progressive-relapsing MS. Relapsing-remitting multiple sclerosis generally occurs in younger people and is the most common form of MS. Symptoms flare up for several days and then go into remission over the next four to eight weeks. The latter three forms (primary-progressive, secondary-progressive, and progressive-relapsing MS) generally fall under the category of chronic-progressive MS. In chronic-progressive MS the symptoms of the disease continue to worsen slowly without remission. About 20% of multiple sclerosis patients (usually those patients whose first symptoms occur after age 45) have the chronic-progressive form of MS without first developing relapsing-remitting MS. Chronic-progressive MS may lead to serious speech problems and paralysis, and generally the symptoms continue to worsen over time.

[0059] Multiple sclerosis is defined as an autoimmune disease; that is, the body's immune system is damaged by genetic or environmental factors or both, causing it to attack its own tissues. In the case of MS, these tissues are the myelin covering the nerve fibers in the brain.

[0060] A symptom of MS is any physical characteristic associated with the disease process. For example, the first symptom of MS is often optic neuritis, the inflammation of the optic nerve. Vision, usually in one eye, becomes unclear or doubled, and there may be a shimmering effect. Pain or nystagmus, involuntary jerking or movement of the eye, may also occur. In 20% of people with this condition, MS develops within two years; in 45% to 80% it develops within 15 years. Other early symptoms of multiple sclerosis include fatigue, heaviness or clumsiness in the arms and legs, tingling sensations, and poor coordination. Another indication of MS is a reaction known as Llermitte's sign, whereby bending the neck produces an electrical sensation that runs down the back and into the legs.

[0061] As the disease develops over months or even years, other symptoms may include spasticity, imbalance, tremors, incontinence, constipation, sexual dysfunction, hearing loss, vertigo, facial pain, and difficulties in swallowing. Problems in speech may occur because of difficulty in controlling the quality of the voice and articulating words. About half of patients display changes in mental function, including problems in concentration and problem solving. In about 10% of cases, there is severe mental dysfunction which resembles dementia. One of the primary symptoms of MS is spasticity, which is characterized by weakness, loss of dexterity, and the inability to control specific movements.

[0062] Myelin: A coating of nerve cells (neurons) made from layers of cell membranes that are produced in the brain and spinal cord by specialized cells called oligodendrocytes. Myelin coats lie in segments along the axons, the long filaments that carry electric impulses away from a nerve cell. The segments are separated from each other by tiny clusters called nodes of Ranvier, which house channels for sodium ions. These sodium ions are important for boosting the electrical charge required to pass signals from one nerve to another.

[0063] Non-human primate: Simian primates including chimpanzees, orangutans, baboons, and macaques. Any non-human primate may be used to produce a KSHV-disease animal model or a JMHV-disease animal model by the methods disclosed herein. Thus, in addition to the rhesus macaque and Japanese macaque models described in detail below, pigtail and cynomologus macaques and baboons may also be used to produce KSHV-disease or JMHV-disease animal models by the methods disclosed herein.

[0064] Oligonucleotide: A linear polynucleotide sequence of up to about 200 nucleotide bases in length, for example a polynucleotide (such as DNA or RNA) which is at least 6 nucleotides, for example at least 15, 25, 50, 100 or even 200 nucleotides long.

[0065] Operably linked: A first nucleic acid sequence is operably linked with a second nucleic acid sequence when the first nucleic acid sequence is placed in a functional relationship with the second nucleic acid sequence. For instance, a promoter is operably linked to a coding sequence if the promoter affects the transcription or expression of the coding sequence. Generally, operably linked DNA sequences are contiguous and, where necessary to join two protein coding regions, in the same reading frame.

[0066] ORF: Open reading frame. Contains a series of nucleotide triplets (codons) coding for amino acids without any termination codons. These sequences are usually translatable into protein.

[0067] PCR: Polymerase chain reaction. Describes a technique in which cycles of denaturation, annealing with primer, and then extension with DNA polymerase are used to amplify the number of copies of a target DNA sequence.

[0068] Polypeptide: A polymer in which the monomers are amino acid residues that are joined together through amide bonds. When the amino acids are alpha-amino acids, either the L-optical isomer or the D-optical isomer can be used, the L-isomers being preferred. The terms “polypeptide” or “protein” as used herein is intended to encompass any amino acid sequence and include modified sequences such as glycoproteins. The term “polypeptide” is specifically intended to cover naturally occurring proteins, as well as those that are recombinantly or synthetically produced.

[0069] The term “fragment” refers to a portion of a polypeptide that is at least 8, 10, 15, 20 or 25 amino acids in length. The term “functional fragments of a polypeptide” refers to all fragments of a polypeptide that retain an activity of the polypeptide (e.g., the binding of an antigen). Biologically functional fragments, for example, can vary in size from a polypeptide fragment as small as an epitope capable of binding an antibody molecule to a large polypeptide capable of participating in the characteristic induction or programming of phenotypic changes within a cell. The term “soluble” refers to a form of a polypeptide that is not inserted into a cell membrane.

[0070] Polypeptide modifications: JMHV polypeptides include synthetic embodiments of polypeptides described herein. In addition, analogs (non-peptide organic molecules), derivatives (chemically functionalized peptide molecules obtained starting with the disclosed polypeptide sequences) and variants (homologs) of these proteins can be utilized in the methods described herein. Each polypeptide of the disclosure is comprised of a sequence of amino acids, which may be either L- and/or D-amino acids, naturally occurring and otherwise.

[0071] Polypeptides may be modified by a variety of chemical techniques to produce derivatives having essentially the same activity as the unmodified polypeptides, and optionally having other desirable properties. For example, carboxylic acid groups of the protein, whether carboxyl-terminal or side chain, may be provided in the form of a salt of a pharmaceutically-acceptable cation or esterified to form a C₁-C₁₆ ester, or converted to an amide of formula NR₁R₂ wherein R₁ and R₂ are each independently H or C₁-C₁₆ alkyl, or combined to form a heterocyclic ring, such as a 5- or 6-membered ring. Amino groups of the peptide, whether amino-terminal or side chain, may be in the form of a pharmaceutically-acceptable acid addition salt, such as the HCl, HBr, acetic, benzoic, toluene sulfonic, maleic, tartaric, and other organic salts, or may be modified to C₁-C₁₆ alkyl or dialkyl amino or further converted to an amide.

[0072] Hydroxyl groups of the peptide side chains may be converted to C₁-C₁₆ alkoxy or to a C₁-C₁₆ ester using well-recognized techniques. Phenyl and phenolic rings of the peptide side chains may be substituted with one or more halogen atoms, such as fluorine, chlorine, bromine, or iodine, or with C₁-C₁₆ alkyl, C₁-C₁₆ alkoxy, carboxylic acids and esters thereof, or amides of such carboxylic acids. Methylene groups of the peptide side chains can be extended to homologous C₂-C₄ alkylenes. Thiols can be protected with any one of a number of well-recognized protecting groups, such as acetamide groups. Those skilled in the art will also recognize methods for introducing cyclic structures into the peptides of this disclosure to select and provide conformational constraints to the structure that result in enhanced stability.

[0073] Peptidomimetic and organomimetic embodiments are envisioned, whereby the three-dimensional arrangement of the chemical constituents of such peptido- and organomimetics mimic the three-dimensional arrangement of the peptide backbone and component amino acid side chains, resulting in such peptido- and organomimetics of a L. longipalpis polypeptide having measurable or enhanced ability to generate an immune response. For computer modeling applications, a pharmacophore is an idealized, three-dimensional definition of the structural requirements for biological activity. Peptido- and organomimetics can be designed to fit each pharmacophore with current computer modeling software (using computer assisted drug design or CADD). See Walters, “Computer-Assisted Modeling of Drugs,” Klegerman & Groves (eds.), 1993, Pharmaceutical Biotechnology, Interpharm Press: Buffalo Grove, Ill., pp. 165-174 and Principles of Pharmacology Munson (ed.) 1995, Ch. 102, for descriptions of techniques used in CADD. Also included are mimetics prepared using such techniques.

[0074] Pharmaceutically acceptable carriers: The pharmaceutically acceptable carriers useful in this disclosure include conventional carriers. Remington's Pharmaceutical Sciences, by E. W. Martin, Mack Publishing Co., Easton, Pa., 15th Edition (1975), describes compositions and formulations suitable for pharmaceutical delivery of the viruses, nucleic acids and/or proteins herein disclosed.

[0075] In general, the nature of the carrier will depend on the particular mode of administration being employed. For instance, parenteral formulations usually comprise injectable fluids that include pharmaceutically and physiologically acceptable fluids such as water, physiological saline, balanced salt solutions, aqueous dextrose, glycerol, ethanol, combinations thereof, or the like, as a vehicle. The carrier and composition can be sterile, and the formulation suits the mode of administration. For solid compositions (e.g., powder, pill, tablet, or capsule forms), conventional non-toxic solid carriers can include, for example, pharmaceutical grades of mannitol, lactose, starch, sodium saccharine, cellulose, magnesium carbonate, or magnesium stearate. In addition to biologically-neutral carriers, pharmaceutical compositions to be administered can contain minor amounts of non-toxic auxiliary substances, such as wetting or emulsifying agents, preservatives, and pH buffering agents and the like, for example sodium acetate or sorbitan monolaurate.

[0076] The composition can be a liquid solution, suspension, emulsion, tablet, pill, capsule, sustained release formulation, or powder. The composition can be formulated as a suppository, with traditional binders and carriers such as triglycerides.

[0077] Probes and primers: Nucleic acid probes and primers may readily be prepared based on the amino acid sequences provided by this disclosure. A probe is an isolated nucleic acid attached to a detectable label or reporter molecule. Typical labels include radioactive isotopes, ligands, fluorescent molecules, chemiluminescent molecules, and enzymes. In other embodiments, labels include co-factors, enzyme substrates; and haptens.

[0078] Methods for labeling and guidance in the choice of labels appropriate for various purposes are discussed, e.g., in Sambrook et al., in Molecular Cloning: A Laboratory Manual, Cold Spring (1989) and Ausubel et al., in Current Protocols in Molecular Biology, Greene Publishing Associates and Wiley-Intersciences (1987).

[0079] Primers are short nucleic acids, such as DNA oligonucleotides 10 nucleotides or more in length. Primers may be annealed to a complementary target DNA strand by nucleic acid hybridization to form a hybrid between the primer and the target DNA strand, and then extended along the target DNA strand by a DNA polymerase enzyme. Primer pairs can be used for amplification of a nucleic acid sequence, e.g., by the polymerase chain reaction (PCR) or other nucleic-acid amplification methods known in the art.

[0080] Methods for preparing and using probes and primers are described, for example, in Sambrook et al. (Molecular Cloning: A Laboratory Manual, 2^(nd) ed., vol. 1-3, Cold Spring Harbor, N.Y. 1989); Ausubel et al. (Current Protocols in Molecular Biology, Greene Publ. Assoc. & Wiley-Intersciences. 1987) and Innis et al. (PCR Protocols, A Guide to Methods and Applications, 1990, Innis et al. (eds.), 21-27, Academic Press, Inc., San Diego, Calif.). PCR primer pairs can be derived from a known sequence, for example, by using computer programs intended for that purpose such as Primer (Version 0.5, © 1991, Whitehead Institute for Biomedical Research, Cambridge, Mass.).

[0081] Probes and primers as used in the present disclosure typically comprise at least 15 contiguous nucleotides of the RRV genome sequence (SEQ ID NO: 1), or 15 contiguous nucleotides of a JMHV sequence. One of skill in the art will appreciate that the specificity of a particular probe or primer increases with its length. Thus, for example, a primer comprising 20 consecutive nucleotides will anneal to a target with a higher specificity than a corresponding primer of only 15 nucleotides. Thus, in order to obtain greater specificity, probes and primers may be selected that comprise 20, 25, 30, 35, 40, 50 or more consecutive nucleotides. In order to enhance specificity, longer probes and primers may also be employed, such as probes and primers that comprise at least 20, 30, 40, 50, 60, 70, 80, 90, 100, or 150 consecutive nucleotides of the disclosed nucleic acid sequences.

[0082] Alternatively, such probes and primers may comprise at least 15, 20, 30, 40, 50, 60, 70, 80, 90, 100, or 150 consecutive nucleotides that share a defined level of sequence identity with the disclosed RRV or JMHV sequence, for instance, at least a 60%, 70%, 80%, 90%, 95% or 98% sequence identity. Alternatively, such probes and primers may be nucleotide molecules which hybridize under wash conditions of 70° C. and about 0.2×SSC for 1 hour, or alternatively under less stringent conditions of 65° C., 60° C., or 55° C. with from about 0.2 to 2×SSC (with, for instance, about 0.1% SDS) for 1 hour with a portion of the JMHV sequence.

[0083] Protein Purification: The JMHV polypeptides disclosed herein can be purified by any of the means known in the art. See, e.g., Guide to Protein Purification, ed. Deutscher, Meth. Enzymol. 185, Academic Press, San Diego, 1990; and Scopes, Protein Purification: Principles and Practice, Springer Verlag, New York, 1982. Substantial purification denotes purification from other proteins or cellular components. A substantially purified protein is at least 60%, 70%, 80%, 90%, 95% or 98% pure. Thus, in one specific, non-limiting example, a substantially purified protein is 90% free of other proteins or cellular components.

[0084] Purified (Isolated): The term purified or isloated does not require absolute purity; rather, it is intended as a relative term. Thus, for example, a purified peptide preparation is one in which the peptide or protein is more enriched than the peptide or protein is in its natural environment within a cell. Preferably, a preparation is purified such that the protein or peptide represents at least 50% of the total peptide or protein content of the preparation.

[0085] Recombinant: A recombinant nucleic acid is one that has a sequence that is not naturally occurring or has a sequence that is made by an artificial combination of two otherwise separated segments of sequence. This artificial combination is often accomplished by chemical synthesis or, more commonly, by the artificial manipulation of isolated segments of nucleic acids, e.g., by genetic engineering techniques.

[0086] RRV 17577: Rhesus macaque rhadinovirus RRV isolate 17577. A Budapest Treaty deposit of RRV 17577 was made with the American Type Culture Collection, Manassas, Va., on Mar. 12, 1998, and has been accorded ATCC Accession No. VR-2601. This virus may be grown on primary rhesus fibroblasts, as described below (see Examples 1 and 14), using standard virological techniques. Alternatively, it may be grown on commercially available rhesus cell lines, including those available from ATCC, such as ATCC CRL-6306 and ATCC CL-160. Infection of a non-human primate with RRV 17577 may be accomplished using any standard method, including intravenous injection (see Examples 13, 23 and 24). Typically, infection is achieved by intravenous injection of around 106 plaque forming units (PFUs) of RRV 17577.

[0087] Rhesus Macaque Rhadinovirus (RRV): A virus having the virological and immunological characteristics of RRV 17577, which causes Kaposi's sarcoma-like disease and lymphoma in infected immunocompromised rhesus monkeys (see published PCT Application No. WO 00/28040 and U.S. patent application Ser. No. 09/831,000, filed May 2, 2001, which are both incorporated by reference herein).

[0088] Sequence Identity: The similarity between two nucleic acid sequences, or two amino acid sequences, is expressed in terms of the similarity between the sequences, otherwise referred to as sequence identity. Sequence identity is frequently measured in terms of percentage identity (or similarity or homology); the higher the percentage, the more similar the two sequences are. Homologs or orthologs of nucleic acid or amino acid sequences will possess a relatively high degree of sequence identity when aligned using standard methods. This homology will be more significant when the orthologous proteins or nucleic acids are derived from species which are more closely related (e.g., human and chimpanzee sequences), compared to species more distantly related (e.g., human and C. elegans sequences). Typically, orthologs are at least 50% identical at the nucleotide level and at least 50% identical at the amino acid level when comparing human orthologous sequences.

[0089] Methods of alignment of sequences for comparison are well known. Various programs and alignment algorithms are described in: Smith & Waterman, Adv. Appl. Math. 2:482, 1981; Needleman & Wunsch, J. Mol. Biol. 48:443, 1970; Pearson & Lipman, Proc. Natl. Acad. Sci. USA 85:2444, 1988; Higgins & Sharp, Gene, 73:237-44, 1988; Higgins & Sharp, CABIOS 5:151-3, 1989; Corpet et al., Nuc. Acids Res. 16:10881-90, 1988; Huang et al., Computer Appls. Biosci. 8:155-65, 1992; and Pearson et al., Meth. Mol. Bio. 24:307-31, 1994. Altschul et al., J. Mol. Biol. 215:403-10, 1990, presents a detailed consideration of sequence alignment methods and homology calculations.

[0090] The NCBI Basic Local Alignment Search Tool (BLAST) (Altschul et al., J. Mol. Biol. 215:403-10, 1990) is available from several sources, including the National Center for Biotechnology Information (NCBI, Bethesda, Md.) and on the Internet, for use in connection with the sequence analysis programs blastp, blastn, blastx, tblastn and tblastx. Each of these sources also provides a description of how to determine sequence identity using this program.

[0091] Homologous sequences are typically characterized by possession of at least 60%, 70%, 75%, 80%, 90%, 95% or at least 98% sequence identity counted over the full length alignment with a sequence using the NCBI Blast 2.0, gapped blastp set to default parameters. Queries searched with the blastn program are filtered with DUST (Hancock and Armstrong, Comput. Appl. Biosci. 10:67-70, 1994). It will be appreciated that these sequence identity ranges are provided for guidance only; it is entirely possible that strongly significant homologs could be obtained that fall outside of the ranges provided.

[0092] Nucleic acid sequences that do not show a high degree of identity may nevertheless encode similar amino acid sequences, due to the degeneracy of the genetic code. It is understood that changes in nucleic acid sequence can be made using this degeneracy to produce multiple nucleic acid sequences that all encode substantially the same protein.

[0093] One indication that two nucleic acid sequences are substantially identical is that the polypeptide encoded by the first nucleic acid is immunologically cross reactive with the polypeptide encoded by the second nucleic acid.

[0094] An alternative indication that two nucleic acid molecules are closely related is that the two molecules hybridize to each other under stringent conditions, as described under “specific hybridization.”

[0095] Homologs of the disclosed RRV or JMHV nucleic acids typically possess at least 50% sequence identity counted over the length of one of the nucleic acids (the reference nucleic acid) using the NCBI Blast 2.0.6, gapped blastn set to default parameters. Nucleic acids showing substantial similarity when assessed by this method may show, for example, at least 50%, 60%, 70%, 80%, 90%, 95% or even 98% or greater sequence identity. When less than the entire sequence is being compared for sequence identity, substantially similar nucleotide sequences will typically possess at least 70% sequence identity over short windows of 30-90 nucleic acids, and may possess sequence identities of at least 80%, 90%, 95% or 98% or greater.

[0096] Homologs of the disclosed RRV or JMHV proteins typically possess at least 50% sequence identity counted over full-length alignment with the amino acid sequence of RRV using the NCBI Blast 2.0, gapped blastp set to default parameters. For comparisons of amino acid sequences of greater than about 30 amino acids, the Blast 2 sequences function is employed using the default BLOSUM62 matrix set to default parameters, (gap existence cost of 11, and a per residue gap cost of 1). When aligning short peptides (fewer than around 30 amino acids), the alignment should be performed using the Blast 2 sequences function, employing the PAM30 matrix set to default parameters (open gap 9, extension gap 1 penalties). Proteins with even greater similarity to the reference sequence will show increasing percentage identities when assessed by this method, such as at least 50%, at least 55%, at least 60%, at least 70%, at least 75%, at least 80%, at least 90%, at least 95%, at least 98%, or at least 99% sequence identity. When less than the entire sequence is being compared for sequence identity, homologs will typically possess at least 70% sequence identity over short windows of 10-20 amino acids, and may possess sequence identities of at least 75%, at least 85% or at least 90%, at least 95% or 98% depending on their similarity to the reference sequence.

[0097] When comparing degrees of sequence identity between similar proteins, the degree of identity will be equal to or less than that the degree of similarity, due to the fact the similarity takes into account conservative amino acid substitutions. So, for instance, the degree of sequence identity between to substantially similar proteins may be at least 50%, 55%, 65%, 75%, 85%, 95%, 98% or more.

[0098] One of ordinary skill in the art will appreciate that these sequence identity ranges are provided for guidance only; it is entirely possible that strongly significant homologs could be obtained that fall outside of the ranges provided. The present disclosure provides not only the peptide homologs that are described above, but also nucleic acid molecules that encode such homologs.

[0099] An alternative indication that two nucleic acid molecules are closely related is that the two molecules hybridize to each other under stringent conditions. In nucleic acid hybridization reactions, the conditions used to achieve a particular level of stringency will vary, depending on the nature of the nucleic acids being hybridized. For example, the length, degree of complementarity, nucleotide sequence composition (e.g., GC v. AT content), and nucleic acid type (e.g., RNA v. DNA) of the hybridizing regions of the nucleic acids can be considered in selecting hybridization conditions. An additional consideration is whether one of the nucleic acids is immobilized, for example, on a filter.

[0100] Specific hybridization: Specific hybridization refers to the binding, duplexing, or hybridizing of a molecule only or substantially only to a particular nucleotide sequence when that sequence is present in a complex mixture (e.g. total cellular DNA or RNA). Specific hybridization may also occur under conditions of varying stringency.

[0101] A specific, non-limiting example of progressively higher stringency conditions is as follows: 2×SSC/0.1% SDS at about room temperature (hybridization conditions); 0.2×SSC/0.1% SDS at about room temperature (low stringency conditions); 0.2×SSC/0.1% SDS at about 42° C. (moderate stringency conditions); and 0.1×SSC at about 68° C. (high stringency conditions). One of skill in the art can readily determine variations on these conditions (for example, Molecular Cloning: A Laboratory Manual, 2nd ed., vol. 1-3, ed. Sambrook et al., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989). The hydridization conditions can be carried out over 2 to 16 hours. Washing can be carried out using only one of the above conditions, for example, high stringency conditions, or each of the conditions can be used, for example, for 10-15 minutes each, in the order listed above, repeating any or all of the steps listed. However, as mentioned above, optimal conditions will vary, depending on the particular hybridization reaction involved, and can be determined empirically.

[0102] Specific binding agent: An agent that binds substantially only to a defined target. As used herein, the term “JMHV peptide specific binding agent” includes anti-JMHV peptide antibodies and other agents that bind substantially only to the JMH peptide. The antibodies may be monoclonal or polyclonal antibodies that are specific for a JMHV peptide, as well as immunologically effective portions (“fragments”) thereof.

[0103] In one embodiment, the antibodies are monoclonal antibodies (or immunologically effective portions thereof) and may also be humanized monoclonal antibodies (or immunologically effective portions thereof). Immunologically effective portions of monoclonal antibodies include Fab, Fab′, F(ab′)₂, Fabc and Fv portions (for a review, see Better and Horowitz, Methods. Enzymol. 178:476-96, 1989). Anti-inhibitory peptide antibodies may also be produced using standard procedures described in a number of texts, including Antibodies, A Laboratory Manual by Harlow and Lane, Cold Spring Harbor Laboratory (1988).

[0104] Methods of making humanized monoclonal antibodies are well known, and include those described in U.S. Pat. No. 5,585,089; U.S. Pat. No. 5,565,332; U.S. Pat. No. 5,225,539; U.S. Pat. No. 5,693,761; U.S. Pat. No. 5,693,762; U.S. Pat. No. 5,585,089; and U.S. Pat. No. 5,530,101 and references cited therein. Similarly, methods of making and using immunologically effective portions of monoclonal antibodies, also referred to as antibody fragments, are well known and include those described in Better and Horowitz, Meth. Enzymol. 178:176-496, 1989; Better et al., 1990, Better and Horowitz, 1990, Advances in Gene technology: The Molecular Biology of Immune Disease & the Immune Response (ICSU Short Reports); Glockshuber et al., Biochemistry 29:1362-7, 1990; and U.S. Pat. No. 5,648,237; U.S. Pat. No. 4,946,778 and U.S. Pat. No. 5,455,030, and references cited therein.

[0105] The determination that a particular agent binds substantially only to a JMHV peptide may readily be made by using or adapting routine procedures. One suitable in vitro assay makes use of the Western blotting procedure (described in many standard texts, including Antibodies, A Laboratory Manual by Harlow and Lane). Western blotting may be used to determine that a given JMHV peptide binding agent, binds substantially only to the specific JMHV protein.

[0106] Supernatant: The culture medium in which a cell is grown. The culture medium includes material from the cell. If the cell is infected with a virus, the supernatant can include viral particles.

[0107] Subject: This term includes both human and non-human subjects. Similarly, the term “patient” includes both human and veterinary subjects. In one embodiment, the subject has multiple sclerosis.

[0108] Symptom and sign: Any subjective evidence of disease or of a subject's condition, i.e., such evidence as perceived by the subject; a noticeable change in a subject's condition indicative of some bodily or mental state. A “sign” is any abnormality indicative of disease, discoverable on examination or assessment of a subject. A sign is generally an objective indication of disease. Signs include, but are not limited to any measurable parameters such as tests for immunological status or the presence of lesions in a subject with multiple sclerosis.

[0109] Therapeutically Effective Amount: A dose sufficient to prevent advancement, or to cause regression of the disease, or which is capable of reducing symptoms caused by the disease, such as multiple sclerosis.

[0110] Transduced: A transduced cell is a cell into which has been introduced a nucleic acid molecule by molecular biology techniques. As used herein, the term transduction encompasses all techniques by which a nucleic acid molecule might be introduced into such a cell, including transfection with viral vectors, transformation with plasmid vectors, and introduction of naked DNA by electroporation, lipofection, and particle gun acceleration.

[0111] Transgenic Cell: Transformed cells which contain foreign, non-native DNA.

[0112] Variants of Amino Acid and Nucleic Acid Sequences: The production of RRV or JMHV proteins can be accomplished in a variety of ways (for example see Examples 17, 21 and 25). DNA sequences which encode the protein, or a fragment of the protein, can be engineered such that they allow the protein to be expressed in eukaryotic cells, bacteria, insects, and/or plants. In order to accomplish this expression, the DNA sequence can be altered and operably linked to other regulatory sequences. The final product, which contains the regulatory sequences and the therapeutic protein, is referred to as a vector. This vector can then be introduced into the eukaryotic cells, bacteria, insect, and/or plant. Once inside the cell the vector allows the protein to be produced.

[0113] One of ordinary skill in the art will appreciate that the DNA can be altered in numerous ways without affecting the biological activity of the encoded protein. For example, PCR may be used to produce variations in the DNA sequence which encodes JMHV proteins. Such variants may be variants that are optimized for codon preference in a host cell that is to be used to express the protein, or other sequence changes that facilitate expression.

[0114] Two types of cDNA sequence variant may be produced. In the first type, the variation in the cDNA sequence is not manifested as a change in the amino acid sequence of the encoded polypeptide. These silent variations are simply a reflection of the degeneracy of the genetic code. In the second type, the cDNA sequence variation does result in a change in the amino acid sequence of the encoded protein. In such cases, the variant cDNA sequence produces a variant polypeptide sequence. In order to preserve the functional and immunologic identity of the encoded polypeptide, it is preferred that any such amino acid substitutions are conservative. Conservative substitutions replace one amino acid with another amino acid that has some homology in size, hydrophobicity, etc. Such substitutions generally are conservative when it is desired to finely modulate the characteristics of the protein. For example, conservative substitutions generally maintain (a) the structure of the polypeptide backbone in the area of the substitution, for example, as a sheet or helical conformation, (b) the charge or hydrophobicity of the molecule at the target site, or (c) the bulk of the side chain.

[0115] Examples of amino acids which may be substituted for an original amino acid in a protein and which are regarded as conservative substitutions include: Ser for Ala; Lys for Arg; Gln or His for Asn; Glu for Asp; Ser for Cys; Asn for Gln; Asp for Glu; Pro for Gly; Asn or Gln for His; Leu or Val for Ile; Ile or Val for Leu; Arg or Gln for Lys; Leu or Ile for Met; Met, Leu or Tyr for Phe; Thr for Ser; Ser for Thr; Tyr for Trp; Trp or Phe for Tyr; and Ile or Leu for Val.

[0116] The substitutions which in general are expected to produce the greatest changes in protein properties will be non-conservative, for instance changes in which (a) a hydrophilic residue, e.g., seryl or threonyl, is substituted for (or by) a hydrophobic residue, e.g., leucyl, isoleucyl, phenylalanyl, valyl or alanyl; (b) a cysteine or proline is substituted for (or by) any other residue; (c) a residue having an electropositive side chain, e.g., lysyl, arginyl, or histadyl, is substituted for (or by) an electronegative residue, e.g., glutamyl or aspartyl; or (d) a residue having a bulky side chain, e.g., phenylalanine, is substituted for (or by) one not having a side chain, e.g., glycine.

[0117] Variations in the DNA sequence that result in amino acid changes, whether conservative or not, should be minimized in order to preserve the functional and immunologic identity of the encoded protein. The immunologic identity of the protein may be assessed by determining whether it is recognized by an antibody to an RRV (or JMHV) protein; a variant that is recognized by such an antibody is immunologically conserved. Any DNA sequence variant will preferably introduce no more than 20, and preferably fewer than 10 amino acid substitutions into the encoded polypeptide. Variant amino acid sequences can, for example, be 80%, 90%, 95% or even 98% identical to the native amino acid sequence.

[0118] Vector: A nucleic acid molecule as introduced into a host cell, thereby producing a transformed host cell. A vector may include nucleic acid sequences that permit it to replicate in the host cell, such as an origin of replication. A vector may also include one or more selectable marker genes and other genetic elements known in the art.

[0119] Virion: A complete viral particle including envelope, capsid (if any), and nucleic acid elements.

[0120] The present disclosure utilizes standard laboratory practices for the cloning, manipulation and sequencing of nucleic acids, purification and analysis of proteins and other molecular biological and biochemical techniques, unless otherwise stipulated. Such techniques are explained in detail in standard laboratory manuals such as Sambrook et al. (Molecular Cloning: A Laboratory Manual, 2^(nd) ed., vol. 1-3, Cold Spring Harbor, N.Y., 1989) and Ausubel et al. (Current Protocols in Molecular Biology, Greene Publ. Assoc. & Wiley-Intersciences, 1987).

[0121] Unless otherwise explained, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. The singular terms “a,” “an,” and “the” include plural referents unless context clearly indicates otherwise. Similarly, the word “or” is intended to include “and” unless the context clearly indicates otherwise. It is further to be understood that all base sizes or amino acid sizes, and all molecular weight or molecular mass values, given for nucleic acids or polypeptides are approximate, and are provided for description. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of this disclosure, suitable methods and materials are described below. The term “comprises” means “includes.” All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including explanations of terms, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

Polynucleotides and Polypeptides

[0122] The sequence of a JMHV is disclosed herein (see SEQ ID NO: 1). Homologous nucleic acid sequences including an nucleic acid sequence at least about 90%, 95%, 98%, or 99% identical to the nucleic acid sequence as set forth in SEQ ID NO: 1 are also disclosed herein. Polynucleotides encoding a JMHV polypeptide (encoded by an open reading frame, or ORF) are also provided, and are termed JMHV polynucleotides. These polynucleotides include DNA, cDNA and RNA sequences which encode a JMHV polypeptide, or encode a polypeptide at least about 85%, at least about 90%, at least about 95%, at least about 98%, or at least about 99% homologous to the JMHV ORF (see Table 3). Specific, non-limiting examples of a JMHV nucleic acid encoding a ORF are nucleic acid 21845 to nucleic acid 22120 of SEQ ID NO: 1 (JMHV25), nucleic acid 22363 to nucleic acid 22701 of SEQ ID NO: 1 (JMHV26), nucleic acid 33254 to nucleic acid 33553 of SEQ ID NO: 1 (JMHV39), nucleic acid 35301 to nucleic acid 35687 of SEQ ID NO: 1 (JMVH41), nucleic acid 40188 to nucleic acid 40439 of SEQ ID NO: 1 (JMHV48), nucleic acid 45836 to nucleic acid 46195 of SEQ ID NO: 1 (JMHV54), nucleic acid 47768 to nucleic acid 48136 of SEQ ID NO: 1 (JM57), nucleic acid 57325 to nucleic acid 57573 of SEQ ID NO: 1 (JM71), nucleic acid 62823 to nucleic acid 63086 of SEQ ID NO: 1 (JM76), nucleic acid 65629 to nucleic acid 65880 of SEQ ID NO: 1 (JM80), nucleic acid 67920 to nucleic acid 68594 of SEQ ID NO: 1 (JM85), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM87), nucleic acid 70328 to nucleic acid 70606 of SEQ ID NO: 1 (JM88), nucleic acid 75447 to nucleic acid 75722 of SEQ ID NO: 1 (JM95), nucleic acid 105581 to nucleic acid 106003 of SEQ ID NO: 1 (JM132), nucleic acid 117501 to nucleic acid 118265 of SEQ ID NO: 1 (JM152), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM159), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM166), and nucleic acid to nucleic acid of SEQ ID NO: 1 (JM167).

[0123] It is understood that all polynucleotides encoding a JMHV polypeptide are also included herein, as long as they encode a polypeptide with the recognized activity, such as the binding to an antibody that recognizes the JMHV polypeptide. The JMHV polynucleotides include sequences that are degenerate as a result of the genetic code. There are 20 natural amino acids, most of which are specified by more than one codon. Therefore, all degenerate nucleotide sequences are included as long as the amino acid sequence of the JMHV polypeptide encoded by the nucleotide sequence is functionally unchanged.

[0124] The JMHV polynucleotides include a recombinant DNA which is incorporated into a vector; into an autonomously replicating plasmid or virus; or into the genomic DNA of a prokaryote or eukaryote, or which exists as a separate molecule (e.g., a cDNA) independent of other sequences. The nucleotides can be ribonucleotides, deoxyribonucleotides, or modified forms of either nucleotide. The term includes single and double forms of DNA. Also included are fragments of the above-described nucleic acid sequences that are at least 15 bases in length, which is sufficient to permit the fragment to selectively hybridize to DNA that encodes the disclosed JMHV polypeptide (such as a polynucleotide that is encoded by SEQ ID NO: 1) under physiological conditions. These nucleic acids can be used as probes or primers for the identification of viral nucleic acid. The term “selectively hybridize” refers to hybridization under moderately or highly stringent conditions, which excludes non-related nucleotide sequences. The JMHV polynucleotide sequence disclosed herein include, but are not limited to, nucleic acid 21845 to nucleic acid 22120 of SEQ ID NO: 1 (JMHV25), nucleic acid 22363 to nucleic acid 22701 of SEQ ID NO: 1 (JMHV26), nucleic acid 33254 to nucleic acid 33553 of SEQ ID NO: 1 (JMHV39), nucleic acid 35301 to nucleic acid 35687 of SEQ ID NO: 1 (JMVH41), nucleic acid 40188 to nucleic acid 40439 of SEQ ID NO: 1 (JMHV48), nucleic acid 45836 to nucleic acid 46195 of SEQ ID NO: 1 (JMHV54), nucleic acid 47768 to nucleic acid 48136 of SEQ ID NO: 1 (JM57), nucleic acid 57325 to nucleic acid 57573 of SEQ ID NO: 1 (JM71), nucleic acid 62823 to nucleic acid 63086 of SEQ ID NO: 1 (JM76), nucleic acid 65629 to nucleic acid 65880 of SEQ ID NO: 1 (J(M80), nucleic acid 67920 to nucleic acid 68594 of SEQ ID NO: 1 (JM85), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM87), nucleic acid 70328 to nucleic acid 70606 of SEQ ID NO: 1 (JM88), nucleic acid 75447 to nucleic acid 75722 of SEQ ID NO: 1 (JM95), nucleic acid 105581 to nucleic acid 106003 of SEQ ID NO: 1 (JM132), nucleic acid 117501 to nucleic acid 118265 of SEQ ID NO: 1 (JM152), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM159), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM166), and nucleic acid to nucleic acid of SEQ ID NO: 1 (JM167).

[0125] The JMHV polypeptides of this disclosure include polypeptides encoded by all of the open reading frames disclosed herein. Polypeptides least 85%, at least about 90%, at least about 95%, at least about 98%, or at least about 99% homologous to the JMHV ORF (see Table 3) are also encompassed by this disclosure. In one embodiment, these polypeptides retain a function of the ORF. The polypeptides also include amino acid sequences including at most one, at most two, at most three, at most four, at most five or at most ten conservative substitutions of the JMHV polypeptide. Fusion proteins are also contemplated that include a heterologous amino acid sequence chemically linked to a JMHV polypeptide. Exemplary fusion proteins include short amino acid sequence tags (such as six histidine residues) as well a fusion of other proteins (such as c-myc or green fluorescent protein fusions). Epitopes of the ORFs, that retain the ability to bind an antibody or to bind the major histocompatibility complex (MHC), and can be used to induce an immune response, are also encompassed by this disclosure. Specific examples of JMHV polypeptides are provided as SEQ ID NOs: 2-171.

[0126] DNA sequences encoding any JMHV polypeptide can be expressed in vitro by DNA transfer into a suitable host cell. The cell may be prokaryotic or eukaryotic. The term also includes any progeny of the subject host cell. It is understood that all progeny may not be identical to the parental cell since there may be mutations that occur during replication. Methods of stable transfer, meaning that the foreign DNA is continuously maintained in the host, are known in the art.

[0127] Polynucleotide sequences encoding an open reading frame of JMHV can be operatively linked to expression control sequences. An expression control sequence operatively linked to a coding sequence is ligated such that expression of the coding sequence is achieved under conditions compatible with the expression control sequences. The expression control sequences include, but are not limited to appropriate promoters, enhancers, transcription terminators, a start codon (i.e., ATG) in front of a protein-encoding gene, splicing signal for introns, maintenance of the correct reading frame of that gene to permit proper translation of mRNA, and stop codons.

[0128] The polynucleotide sequences encoding a JMHV ORF may be inserted into an expression vector including, but not limited to a plasmid, virus or other vehicle that can be manipulated to allow insertion or incorporation of sequences and can be expressed in either prokaryotes or eukaryotes. Hosts can include microbial, yeast, insect and mammalian organisms. Methods of expressing DNA sequences having eukaryotic or viral sequences in prokaryotes are well known in the art. Biologically functional viral and plasmid DNA vectors capable of expression and replication in a host are known in the art.

[0129] Transformation of a host cell with recombinant DNA may be carried out by conventional techniques as are well known to those skilled in the art. Where the host is prokaryotic, such as E. coli, competent cells which are capable of DNA uptake can be prepared from cells harvested after exponential growth phase and subsequently treated by the CaCl₂ method using procedures well known in the art. Alternatively, MgCl₂ or RbCl can be used. Transformation can also be performed after forming a protoplast of the host cell if desired, or by electroporation.

[0130] When the host is a eukaryote, such methods of transfection of DNA as calcium phosphate coprecipitates, conventional mechanical procedures such as microinjection, electroporation, insertion of a plasmid encased in liposomes, or virus vectors may be used. Eukaryotic cells can also be cotransformed with JMHV polynucleotide sequences, and a second foreign DNA molecule encoding a selectable phenotype, such as the herpes simplex thymidine kinase gene. Another method is to use a eukaryotic viral vector, such as simian virus 40 (SV40) or bovine papilloma virus, to transiently infect or transform eukaryotic cells and express the protein (see for example, Eukaryotic Viral Vectors, Cold Spring Harbor Laboratory, Gluzman ed., 1982).

[0131] Isolation and purification of recombinantly expressed polypeptide may be carried out by conventional means including preparative chromatography and immunological separations. The peptides can be chemically synthesized by any of a number of manual or automated methods of synthesis known in the art. For example, solid phase peptide synthesis (SPPS) is carried out on a 0.25 millimole (mmole) scale using an Applied Biosystems Model 431A Peptide Synthesizer and using 9-fluorenylmethyloxycarbonyl (Fmoc) amino-terminus protection, coupling with dicyclohexylcarbodiimide/hydroxybenzotriazole or 2-(1H-benzo-triazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate/hydroxybenzotriazole (HBTU/HOBT), and using p-hydroxymethylphenoxymethylpolystyrene (HMP) or Sasrin resin for carboxyl-terminus acids or Rink amide resin for carboxyl-terminus amides.

[0132] Fmoc-derivatized amino acids are prepared from the appropriate precursor amino acids by tritylation and triphenylmethanol in trifluoroacetic acid, followed by Fmoc derivitization as described by Atherton et al. (Solid Phase Peptide Synthesis, IRL Press: Oxford, 1989).

[0133] Sasrin resin-bound peptides are cleaved using a solution of 1% TFA in dichloromethane to yield the protected peptide. Where appropriate, protected peptide precursors are cyclized between the amino- and carboxyl-termini by reaction of the amino-terminal free amine and carboxyl-terminal free acid using diphenylphosphorylazide in nascent peptides wherein the amino acid sidechains are protected.

[0134] HMP or Rink amide resin-bound products are routinely cleaved and protected sidechain-containing cyclized peptides deprotected using a solution comprised of trifluoroacetic acid (TFA), optionally also comprising water, thioanisole, and ethanedithiol, in ratios of 100:5:5:2.5, for 0.5-3 hours at room temperature.

[0135] Crude peptides are purified by preparative high pressure liquid chromatography (HPLC), for example using a Waters Delta-Pak C18 column and gradient elution with 0.1% TFA in water modified with acetonitrile. After column elution, acetonitrile is evaporated from the eluted fractions, which are then lyophilized. The identity of each product so produced and purified may be confirmed by fast atom bombardment mass spectroscopy (FABMS) or electrospray mass spectroscopy (ESMS).

Antibodies

[0136] A JMHV polypeptide or a fragment or conservative variant thereof can be used to produce antibodies which are immunoreactive or bind to an epitope of the JMHV polypeptide. Polyclonal antibodies, antibodies which consist essentially of pooled monoclonal antibodies with different epitopic specificities, as well as distinct monoclonal antibody preparations are included.

[0137] The preparation of polyclonal antibodies is well-known to those skilled in the art. See, for example, Green et al., “Production of Polyclonal Antisera,” in Immunochemical Protocols pages 1-5, Manson, ed., Humana Press 1992; Coligan et al., “Production of Polyclonal Antisera in Rabbits, Rats, Mice and Hamsters,” in: Current Protocols in Immunology, section 2.4.1, 1992.

[0138] The preparation of monoclonal antibodies likewise is conventional. See, for example, Kohler & Milstein, Nature 256:495, 1975; Coligan et al., sections 2.5.1-2.6.7; and Harlow et al., in: Antibodies: a Laboratory Manual, page 726, Cold Spring Harbor Pub., 1988. Briefly, monoclonal antibodies can be obtained by injecting mice with a composition comprising an antigen, verifying the presence of antibody production by removing a serum sample, removing the spleen to obtain B lymphocytes, fusing the B lymphocytes with myeloma cells to produce hybridomas, cloning the hybridomas, selecting positive clones that produce antibodies to the antigen, and isolating the antibodies from the hybridoma cultures. Monoclonal antibodies can be isolated and purified from hybridoma cultures by a variety of well-established techniques. Such isolation techniques include affinity chromatography with Protein-A Sepharose, size-exclusion chromatography, and ion-exchange chromatography. See, e.g., Coligan et al., sections 2.7.1-2.7.12 and sections 2.9.1-2.9.3; Barnes et al., “Purification of Immunoglobulin G (IgG),” in: Methods in Molecular Biology, Vol. 10, pages 79-104, Humana Press, 1992.

[0139] Methods of in vitro and in vivo multiplication of monoclonal antibodies are well known to those skilled in the art. Multiplication in vitro may be carried out in suitable culture media such as Dulbecco's Modified Eagle Medium or RPMI 1640 medium, optionally supplemented by a mammalian serum such as fetal calf serum or trace elements and growth-sustaining supplements such as normal mouse peritoneal exudate cells, spleen cells, thymocytes or bone marrow macrophages. Production in vitro provides relatively pure antibody preparations and allows scale-up to yield large amounts of the desired antibodies. Large-scale hybridoma cultivation can be carried out by homogenous suspension culture in an airlift reactor, in a continuous stirrer reactor, or in immobilized or entrapped cell culture. Multiplication in vivo may be carried out by injecting cell clones into mammals histocompatible with the parent cells, e.g., syngeneic mice, to cause growth of antibody-producing tumors. Optionally, the animals are primed with a hydrocarbon, especially oils such as pristane (tetramethylpentadecane) prior to injection. After one to three weeks, the desired monoclonal antibody is recovered from the body fluid of the animal.

[0140] Antibodies can also be derived from subhuman primate antibody. General techniques for raising therapeutically useful antibodies in baboons can be found, for example, in WO 91/11465, 1991, and Losman et al., Int. J. Cancer 46:310, 1990.

[0141] Alternatively, an antibody that specifically binds a JMHV polypeptide can be derived from a humanized monoclonal antibody. Humanized monoclonal antibodies are produced by transferring mouse complementarity determining regions from heavy and light variable chains of the mouse immunoglobulin into a human variable domain, and then substituting human residues in the framework regions of the murine counterparts. The use of antibody components derived from humanized monoclonal antibodies obviates potential problems associated with the immunogenicity of murine constant regions. General techniques for cloning murine immunoglobulin variable domains are described, for example, by Orlandi et al., Proc. Nat'l Acad. Sci. U.S.A. 86:3833, 1989. Techniques for producing humanized monoclonal antibodies are described, for example, by Jones et al., Nature 321:522, 1986; Riechmann et al., Nature 332:323, 1988; Verhoeyen et al., Science 239:1534, 1988; Carter et al., Proc. Nat'l Acad. Sci. U.S.A. 89:4285, 1992; Sandhu, Crit. Rev. Biotech. 12:437, 1992; and Singer et al., J. Immunol. 150:2844, 1993.

[0142] Antibodies can be derived from human antibody fragments isolated from a combinatorial immunoglobulin library. See, for example, Barbas et al., in: Methods: a Companion to Methods in Enzymology, Vol. 2, page 119, 1991; Winter et al., Ann. Rev. Immunol. 12:433, 1994. Cloning and expression vectors that are useful for producing a human immunoglobulin phage library can be obtained, for example, from STRATAGENE Cloning Systems (La Jolla, Calif.).

[0143] In addition, antibodies can be derived from a human monoclonal antibody. Such antibodies are obtained from transgenic mice that have been “engineered” to produce specific human antibodies in response to antigenic challenge. In this technique, elements of the human heavy and light chain loci are introduced into strains of mice derived from embryonic stem cell lines that contain targeted disruptions of the endogenous heavy and light chain loci. The transgenic mice can synthesize human antibodies specific for human antigens, and the mice can be used to produce human antibody-secreting hybridomas. Methods for obtaining human antibodies from transgenic mice are described by Green et al., Nature Genet. 7:13, 1994; Lonberg et al., Nature 368:856, 1994; and Taylor et al., Int. Immunol.6:579, 1994.

[0144] Antibodies include intact molecules as well as fragments thereof, such as Fab, F(ab′)₂, and Fv which are capable of binding the epitopic determinant. These antibody fragments retain some ability to selectively bind with their antigen or receptor and are defined as follows:

[0145] (1) Fab, the fragment which contains a monovalent antigen-binding fragment of an antibody molecule, can be produced by digestion of whole antibody with the enzyme papain to yield an intact light chain and a portion of one heavy chain;

[0146] (2) Fab′, the fragment of an antibody molecule can be obtained by treating whole antibody with pepsin, followed by reduction, to yield an intact light chain and a portion of the heavy chain; two Fab′ fragments are obtained per antibody molecule;

[0147] (3) (Fab′)₂, the fragment of the antibody that can be obtained by treating whole antibody with the enzyme pepsin without subsequent reduction; F(ab′)₂ is a dimer of two Fab′ fragments held together by two disulfide bonds;

[0148] (4) Fv, defined as a genetically engineered fragment containing the variable region of the light chain and the variable region of the heavy chain expressed as two chains; and

[0149] (5) Single chain antibody (SCA), defined as a genetically engineered molecule containing the variable region of the light chain, the variable region of the heavy chain, linked by a suitable polypeptide linker as a genetically fused single chain molecule.

[0150] Methods of making these fragments are known in the art. (See for example, Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, New York, 1988). An epitope is any antigenic determinant on an antigen to which the paratope of an antibody binds. Epitopic determinants usually consist of chemically active surface groupings of molecules such as amino acids or sugar side chains and usually have specific three dimensional structural characteristics, as well as specific charge characteristics.

[0151] Antibody fragments can be prepared by proteolytic hydrolysis of the antibody or by expression in E. coli of DNA encoding the fragment. Antibody fragments can be obtained by pepsin or papain digestion of whole antibodies by conventional methods. For example, antibody fragments can be produced by enzymatic cleavage of antibodies with pepsin to provide a 5S fragment denoted F(ab′)₂. This fragment can be further cleaved using a thiol reducing agent, and optionally a blocking group for the sulfhydryl groups resulting from cleavage of disulfide linkages, to produce 3.5S Fab′ monovalent fragments. Alternatively, an enzymatic cleavage using pepsin produces two monovalent Fab′ fragments and an Fc fragment directly (see U.S. Pat. No. 4,036,945 and U.S. Pat. No. 4,331,647, and references contained therein; Nisonhoff et al., Arch. Biochem. Biophys.89:230, 1960; Porter, Biochem. J. 73:119, 1959; Edelman et al., Methods in Enzymology, Vol. 1, page 422, Academic Press, 1967; and Coligan et al. at sections 2.8.1-2.8.10 and 2.10.1-2.10.4).

[0152] Other methods of cleaving antibodies, such as separation of heavy chains to form monovalent light-heavy chain fragments, further cleavage of fragments, or other enzymatic, chemical, or genetic techniques may also be used, so long as the fragments bind to the antigen that is recognized by the intact antibody.

[0153] For example, Fv fragments comprise an association of V_(H) and V_(L) chains. This association may be noncovalent (Inbar et al., Proc. Nat'l Acad. Sci. U.S.A. 69:2659, 1972). Alternatively, the variable chains can be linked by an intermolecular disulfide bond or cross-linked by chemicals such as glutaraldehyde. See, e.g., Sandhu, supra. Preferably, the Fv fragments comprise V_(H) and V_(L) chains connected by a peptide linker. These single-chain antigen binding proteins (sFv) are prepared by constructing a structural gene comprising DNA sequences encoding the V_(H) and V_(L) domains connected by an oligonucleotide. The structural gene is inserted into an expression vector, which is subsequently introduced into a host cell such as E. coli. The recombinant host cells synthesize a single polypeptide chain with a linker peptide bridging the two V domains. Methods for producing sFvs are known in the art (see Whitlow et al., Methods: a Companion to Methods in Enzymology, Vol. 2, page 97, 1991; Bird et al., Science 242:423, 1988; U.S. Pat. No. 4,946,778; Pack et al., Bio/Technology 11:1271, 1993; and Sandhu, supra).

[0154] Another form of an antibody fragment is a peptide coding for a single complementarity-determining region (CDR). CDR peptides (“minimal recognition units”) can be obtained by constructing genes encoding the CDR of an antibody of interest. Such genes are prepared, for example, by using the polymerase chain reaction to synthesize the variable region from RNA of antibody-producing cells (Larrick et al., Methods: a Companion to Methods in Enzymology, Vol. 2, page 106, 1991).

[0155] Antibodies can be prepared using an intact polypeptide or fragments containing small peptides of interest as the immunizing antigen. The polypeptide or a peptide used to immunize an animal can be derived from substantially purified polypeptide produced in host cells, in vitro translated cDNA, or chemical synthesis which can be conjugated to a carrier protein, if desired. Such commonly used carriers which are chemically coupled to the peptide include keyhole limpet hemocyanin (KLH), thyroglobulin, bovine serum albumin (BSA), and tetanus toxoid. The coupled peptide is then used to immunize the animal (e.g., a mouse, a rat, or a rabbit).

[0156] Polyclonal or monoclonal antibodies can be further purified, for example, by binding to and elution from a matrix to which the polypeptide or a peptide to which the antibodies were raised is bound. Those of skill in the art will know of various techniques common in the immunology arts for purification and/or concentration of polyclonal antibodies, as well as monoclonal antibodies (See for example, Coligan et al., Unit 9, Current Protocols in Immunology, Wiley Interscience, 1991).

[0157] It is also possible to use the anti-idiotype technology to produce monoclonal antibodies which mimic an epitope. For example, an anti-idiotypic monoclonal antibody made to a first monoclonal antibody will have a binding domain in the hypervariable region that is the “image” of the epitope bound by the first monoclonal antibody.

[0158] Effector molecules, e.g., therapeutic, diagnostic, or detection moieties, can be linked to an antibody that specifically binds a JMHV polypeptide, using any number of means known to those of skill in the art. Both covalent and noncovalent attachment means may be used. The procedure for attaching an effector molecule to an antibody varies according to the chemical structure of the effector. Polypeptides typically contain a variety of functional groups; e.g., carboxylic acid (COOH), free amine (—NH₂) or sulfhydryl (—SH) groups, which are available for reaction with a suitable functional group on an antibody to result in the binding of the effector molecule. Alternatively, the antibody is derivatized to expose or attach additional reactive functional groups. The derivatization may involve attachment of any of a number of linker molecules such as those available from Pierce Chemical Company, Rockford, Ill. The linker can be any molecule used to join the antibody to the effector molecule. The linker is capable of forming covalent bonds to both the antibody and to the effector molecule. Suitable linkers are well known to those of skill in the art and include, but are not limited to, straight or branched-chain carbon linkers, heterocyclic carbon linkers, or peptide linkers. Where the antibody and the effector molecule are polypeptides, the linkers may be joined to the constituent amino acids through their side groups (such as through a disulfide linkage to cysteine) or to the alpha carbon amino and carboxyl groups of the terminal amino acids.

[0159] In some circumstances, it is desirable to free the effector molecule from the antibody when the immunoconjugate has reached its target site. Therefore, in these circumstances, immunoconjugates will comprise linkages that are cleavable in the vicinity of the target site. Cleavage of the linker to release the effector molecule from the antibody may be prompted by enzymatic activity or conditions to which the immunoconjugate is subjected either inside the target cell or in the vicinity of the target site.

[0160] In view of the large number of methods that have been reported for attaching a variety of radiodiagnostic compounds, radiotherapeutic compounds, label (e.g. enzymes or fluorescent molecules) drugs, toxins, and other agents to antibodies, one skilled in the art will be able to determine a suitable method for attaching a given effector molecule to an antibody or other polypeptide.

[0161] The immunoconjugates can be prepared by cloning techniques. Examples of appropriate cloning and sequencing techniques, and instructions sufficient to direct persons of skill through many cloning exercises are found in Sambrook et al., Molecular Cloning: A Laboratory Manual (2nd Ed.), Vols. 1-3, Cold Spring Harbor Laboratory (1989), Berger and Kimmel (eds.), Guide to Molecular Cloning Techniques, Academic Press, Inc., San Diego Calif. (1987), or Ausubel et al. (eds.), Current Protocols in Molecular Biology, Greene Publishing and Wiley-Interscience, NY (1987). Product information from manufacturers of biological reagents and experimental equipment also provide useful information. Such manufacturers include the SIGMA chemical company (Saint Louis, Mo.), R&D systems (Minneapolis, Minn.), Pharmacia LKB Biotechnology (Piscataway, N.J.), CLONTECH Laboratories, Inc. (Palo Alto, Calif.), Chem Genes Corp., Aldrich Chemical Company (Milwaukee, Wis.), Glen Research, Inc., GIBCO BRL Life Technologies, Inc. (Gaithersburg, Md.), Fluka Chemica-Biochemika Analytika (Fluka Chemie AG, Buchs, Switzerland), Invitrogen (San Diego, Calif.), and Applied Biosystems (Foster City, Calif.), as well as many other commercial sources known to one of skill.

[0162] Nucleic acids encoding native effector molecules or anti-JMHV antibodies can be modified to form the effector molecule, antibodies, or immunoconjugates. Modification by site-directed mutagenesis is well known in the art. Nucleic acids encoding effector molecule or anti-JMHV antibodies can be amplified by in vitro methods. Amplification methods include the polymerase chain reaction (PCR), the ligase chain reaction (LCR), the transcription-based amplification system (TAS), the self-sustained sequence replication system (3SR). A wide variety of cloning methods, host cells, and in vitro amplification methodologies are well known in the art.

[0163] In one embodiment, immunoconjugates are prepared by inserting a cDNA which encodes an anti-JMHV polypeptide scFv antibody into a vector which comprises the cDNA encoding the effector molecule. The insertion is made so that the scFv and the EM are read in frame that is in one continuous polypeptide which contains a functional Fv region and a functional EM region

[0164] In addition to recombinant methods, the immunoconjugates, effector molecules, and antibodies can also be constructed in whole or in part using standard peptide synthesis. Solid phase synthesis of the polypeptides of less than about 50 amino acids in length may be accomplished by attaching the C-terminal amino acid of the sequence to an insoluble support followed by sequential addition of the remaining amino acids in the sequence. Techniques for solid phase synthesis are described by Barany & Merrifield, “The Peptides: Analysis, Synthesis, Biology,” Vol. 2, Special Methods in Peptide Synthesis, Part A. pp. 3-284; Merrifield et al. J. Am. Chem. Soc. 85:2149-2156, 1963, and Stewart et al., Solid Phase Peptide Synthesis, 2nd ed., Pierce Chem. Co., Rockford, Ill., 1984. Proteins of greater length may be synthesized by condensation of the amino and carboxyl termini of shorter fragments. Methods of forming peptide bonds by activation of a carboxyl terminal end (e.g., by the use of the coupling reagent N,N′-dicycylohexylcarbodiimide) are known to those of skill.

[0165] Once the nucleic acids encoding an EM, anti-JMHV antibody, or an immunoconjugate, are isolated and cloned, one may express the desired protein in a recombinantly engineered cell such as bacteria, plant, yeast, insect and mammalian cells. It is expected that those of skill in the art are knowledgeable in the numerous expression systems available for expression of proteins including E. coli, other bacterial hosts, yeast, and various higher eukaryotic cells such as the COS, CHO, HeLa and myeloma cell lines.

[0166] Antibodies can be covalently or non-covalently linked to a detectable label. Detectable labels suitable for such use include any composition detectable by spectroscopic, photochemical, biochemical, immunochemical, electrical, optical or chemical means. Useful labels in the present disclosure include magnetic beads (e.g. DYNABEADS), fluorescent dyes (e.g., fluorescein isothiocyanate, Texas red, rhodamine, green fluorescent protein, and the like), radiolabels (e.g., ³H, ¹²⁵I, ³⁵S, ¹⁴C, or ³²P), enzymes (e.g., horseradish peroxidase, alkaline phosphatase and others commonly used in an ELISA), and calorimetric labels such as colloidal gold or colored glass or plastic (e.g., polystyrene, polypropylene, latex, etc.) beads. Means of detecting such labels are well known to those of skill in the art. Thus, for example, radiolabels may be detected using photographic film or scintillation counters, fluorescent markers may be detected using a photodetector to detect emitted illumination. Enzymatic labels are typically detected by providing the enzyme with a substrate and detecting the reaction product produced by the action of the enzyme on the substrate, and colorimetric labels are detected by simply visualizing the colored label.

Diagnostic Methods

[0167] A method for screening a subject to determine if the subject has been infected with JMHV is disclosed herein. One major application of the JMHV sequence information presented herein is in the area of diagnostic testing for predisposition to a disease (such as for multiple sclerosis) that develops in at least a subset of hosts infected with JMHV. The nucleic acid sequence of the JMHV ORFs is also useful in such diagnostic methods. The method includes providing a biological sample obtained from the subject, in which sample includes DNA or RNA, and providing an assay for detecting in the biological sample the presence of any of the JMHV nucleic acids or proteins. Suitable biological samples include samples obtained from body cells, such as those present in peripheral blood, urine, saliva, tissue biopsy, surgical specimen, fine needle aspirate specimen, amniocentesis samples and autopsy material. The detection in the biological sample may be performed by a number of methodologies, as outlined below.

[0168] The foregoing assay may be assembled in the form of a diagnostic kit and preferably comprises either: hybridization with oligonucleotides; PCR amplification of the gene or a part thereof using oligonucleotide primers; RT-PCR amplification of the RNA or a part thereof using oligonucleotide primers; or direct sequencing of any of the JMHV genes present in a subject using oligonucleotide primers. The efficiency of these molecular genetic methods should permit the rapid identification of patients infected with JMHV. Thus kits can include containers with JMHV nucleic acid sequences (such as probes or primers) and/or containers including an antibody that specifically binds JMHV.

[0169] One embodiment of such detection techniques is the polymerase chain reaction amplification of reverse transcribed RNA (RT-PCR) of RNA isolated from cells (for example lymphocytes) followed by direct DNA sequence determination of the products. The presence of one or more JMHV genes is taken an indicative of potential JMHV infection.

[0170] Alternatively, DNA extracted from lymphocytes or other cells may be used directly for amplification. The direct amplification from genomic DNA would be appropriate for analysis of an entire JMHV nucleic acid sequence including regulatory sequences located upstream and downstream from the open reading frame. Recent reviews of direct DNA diagnosis have been presented by Caskey (Science 236:1223-1228, 1989) and by Landegren et al. (Science 242:229-37, 1989). DNA diagnostic methods to specifically detect an ORF, or to detect a particular polymorphism in an ORF, can be designed.

[0171] The detection of specific DNA mutations or alterations in gene sequences may be achieved by methods such as hybridization using specific oligonucleotides (Wallace et al., Cold Spring Harbor Symp. Quant. Biol. 51:257-61, 1986), direct DNA sequencing (Church and Gilbert, Proc. Natl. Acad. Sci. USA. 81:1991-5, 1984), the use of restriction enzymes (Flavell et al., Cell 15:25, 1978; Geever et al., Proc. Natl. Acad. Sci USA 78:5081, 1981), discrimination on the basis of electrophoretic mobility in gels with denaturing reagent (Myers and Maniatis, Cold Spring Harbor Symp. Quant. Biol. 51:275-284, 1986), RNase protection (Myers et al., Science 230:1242, 1985), chemical cleavage (Cotton et al., Proc. Natl. Acad. Sci. USA 85:4397-401, 1985), and the ligase-mediated detection procedure (Landegren et al., Science 241:1077, 1988).

[0172] Oligonucleotides specific to normal, mutant or alterative sequences are chemically synthesized using commercially available machines, labeled radioactively with isotopes (such as ³²P) or non-radioactively, with tags such as biotin (Ward and Langer et al., Proc. Natl. Acad. Sci. USA 78:6633-57, 1981), and hybridized to individual DNA samples immobilized on membranes or other solid supports by dot-blot or transfer from gels after electrophoresis. The presence of these specific sequences are visualized by methods such as autoradiography or fluorometric (Landegren et al., Science 242:229-37, 1989) or calorimetric reactions (Gebeyehu et al., Nucleic Acids Res. 15:4513-34, 1987). The absence of hybridization would indicate a mutation in the particular region of the gene, or that the patient is not infected with JMHV.

[0173] Sequence differences between disclosed and other forms of JMHV genes may also be revealed by the direct DNA sequencing method of Church and Gilbert (Proc. Natl. Acad. Sci. USA 81:1991-5, 1988). Cloned DNA segments may be used as probes to detect specific DNA segments. The sensitivity of this method is greatly enhanced when combined with PCR (Wrichnik et al., Nucleic Acids Res. 15:529-42, 1987; Wong et al., Nature 330:384-6, 1987; Stoflet et al., Science 239:491-4, 1988). In this approach, a sequencing primer which lies within the amplified sequence is used with double-stranded PCR product or single-stranded template generated by a modified PCR. The sequence determination is performed by conventional procedures with radiolabelled nucleotides or by automatic sequencing procedures with fluorescent tags.

[0174] Sequence alterations may occasionally generate fortuitous restriction enzyme recognition sites or may eliminate existing restriction sites. Changes in restriction sites are revealed by the use of appropriate enzyme digestion followed by conventional gel-blot hybridization (Southern, J. Mol. Biol. 98:503, 1975). DNA fragments carrying the site (either normal, mutant, or alternative) are detected by their reduction in size or increase of corresponding restriction fragment numbers. Genomic DNA samples may also be amplified by PCR prior to treatment with the appropriate restriction enzyme; fragments of different sizes are then visualized under UV light in the presence of ethidium bromide after gel electrophoresis.

[0175] Screening based on DNA sequence differences may be achieved by detection of alteration in electrophoretic mobility of DNA fragments in gels with or without denaturing reagent. Small sequence deletions and insertions can be visualized by high-resolution gel electrophoresis. For example, a PCR product with small deletions is clearly distinguishable from a normal sequence on an 8% non-denaturing polyacrylamide gel (WO 91/10734; Nagamine et al., Am. J. Hum. Genet. 45:337-9, 1989). DNA fragments of different sequence compositions may be distinguished on denaturing formamide gradient gels in which the mobilities of different DNA fragments are retarded in the gel at different positions according to their specific “partial-melting” temperatures (Myers et al., Science 230:1242, 1985). Alternatively, a method of detecting a mutation comprising a single base substitution or other small change could be based on differential primer length in a PCR. For example, an invariant primer could be used in addition to a primer specific for a mutation. The PCR products of the normal and mutant genes can then be differentially detected in acrylamide gels.

[0176] In addition to conventional gel-electrophoresis and blot-hybridization methods, DNA fragments may also be visualized by methods where the individual DNA samples are not immobilized on membranes. The probe and target sequences may be both in solution, or the probe sequence may be immobilized (Saiki et al., Proc. Nat. Acad. Sci. USA 86:6230-4, 1989). A variety of detection methods, such as autoradiography involving radioisotopes, direct detection of radioactive decay (in the presence or absence of scintillant), spectrophotometry involving calorigenic reactions and fluorometry involved fluorogenic reactions, may be used to identify specific individual genotypes.

[0177] If more than one mutation or alternative sequence is frequently encountered in one or more JMHV genes, a system capable of detecting such multiple mutations can be produced. For example, a PCR with multiple, specific oligonucleotide primers and hybridization probes can be used to identify all possible mutations or alternative sequences at the same time (Chamberlain et al., Nucl. Acids Res. 16:1141-55, 1988). The procedure may involve immobilized sequence-specific oligonucleotides probes (Saiki et al., Proc. Nat. Acad. Sci. USA 86:6230-4, 1989).

Quantitation of JMHV Proteins

[0178] An alternative method of determining if a subject has been infected with RRV or JMHV is to quantitate the level of one or more RRV (or JMHV) proteins in the cells of a subject. This diagnostic tool would also be useful for detecting the levels of the JMHV proteins which result from infection by JMHV. These diagnostic methods provide an enhanced ability to diagnose susceptibility to diseases caused by JMHV infection.

[0179] The determination of JMHV protein levels would be an alternative or supplemental approach to the direct determination of the presence of one or more JMHV genes. The availability of antibodies specific to one or more of the JMHV proteins will facilitate the quantitation of cellular JMHV proteins by one of a number of immunoassay methods which are well known in the art and are presented in Harlow and Lane (Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory, New York., 1988).

[0180] Such assays permit the detection of JMHV proteins in a biological sample and the quantitation of such proteins. Typical methods involve: providing a biological sample of the subject in which the sample contains cellular proteins, and providing an immunoassay for quantitating the level of at least one JMHV protein in the biological sample. This can be achieved by combining the biological sample with a JMHV specific binding agent, such as an antibody (e.g. monoclonal or polyclonal antibodies that bind a JMHV protein), so that complexes form between the binding agent and the viral protein present in the sample, and then detecting or quantitating such complexes.

[0181] In particular forms, these assays may be performed with the JMHV specific binding agent immobilized on a support surface, such as in the wells of a microtiter plate or on a column. The biological sample is then introduced onto the support surface and allowed to interact with the specific binding agent so as to form complexes. Excess biological sample is then removed by washing, and the complexes are detected with a reagent, such as a second anti-JMHV protein antibody, that is conjugated with a detectable marker.

[0182] In an alternative assay, the cellular proteins are isolated and subjected to SDS-PAGE followed by Western blotting. After resolving the proteins, the proteins are transferred to a membrane, which is probed with specific binding agents that recognize any of the JMHV proteins. The proteins are detected, for example with labeled (such as horseradish peroxidase, HRP)-conjugated secondary antibodies, and quantitated.

[0183] In yet another assay, the level of one or more JMHV proteins in cells is analyzed using microscopy. Using specific binding agents which recognize JMHV, samples can be analyzed for the presence of one or more JMHV proteins. For example, frozen biopsied tissue sections are thawed at room temperature and fixed with acetone at −200° C. for 5 minutes. Slides are washed twice in cold PBS for 5 minutes each, then air-dried. Sections are covered with 20-30 μl of antibody solution (15-45 μg/ml) (diluted in PBS, 2% BSA at 15-50 μg/ml) and incubated at room temperature in humidified chamber for 30 minutes. Slides are washed three times with cold PBS 5 minutes each, allowed to air-dry briefly (5 minutes) before applying 20-30 μl of the second antibody solution (diluted in PBS, 2% BSA at 15-50 μg/ml) and incubated at room temperature in humidified chamber for 30 minutes. The label on the second antibody may contain a fluorescent probe, enzyme, radiolabel, biotin, or other detectable marker. The slides are washed three times with cold PBS 5 minutes each then quickly dipped in distilled water, air-dried, and mounted with PBS containing 30% glycerol. Slides can be stored at 4° C. prior to viewing.

[0184] For samples prepared for electron microscopy (versus light microscopy), the second antibody is conjugated to gold particles. Tissue is fixed and embedded with epoxy plastics, then cut into very thin sections (˜1-2 μm). The specimen is then applied to a metal grid, which is then incubated in the primary anti-JMHV antibody, washed in a buffer containing BSA, then incubated in a secondary antibody conjugated to gold particles (usually 5-20 nm). These gold particles are visualized using electron microscopy methods.

[0185] For the purposes of quantitating the JMHV proteins, a biological sample of the subject, which sample includes cellular proteins, is required. Such a biological sample may be obtained from body cells, such as those present in which expression of the protein has been detected. The expression of JMHV proteins in peripheral blood leukocytes is clearly the most accessible and convenient source from which specimens can be obtained. Specimens can be obtained from peripheral blood, urine, saliva, tissue biopsy, amniocentesis samples, surgical specimens, fine needle aspirates, and autopsy material, particularly cancer cells. Quantitation of JMHV proteins would be made by immunoassay and compared to levels of the protein found in non-JMHV expressing cells, or to the level of JMHV proteins in non-JMHV infected cells (cells of the same origin that are not infected). A significant (preferably 50% or greater) increase in the amount of one or more JMHV proteins in the cells of a subject compared to the amount of one or more JMHV proteins found in non-JMHV infected cells or that found in normal cells, would be taken as an indication that the subject may have been infected with JMHV.

Screening Assays for Pharmaceutical Agents of Interest

[0186] The present disclosure provides a virus that is involved in the causation or progression of certain diseases, such as multiple sclerosis, and therefore provides an animal model and assays directed to identifying potential pharmaceutical agents that inhibit the biological activity of the virus. Drug screening assays which determine whether or not a drug has activity against the virus can include incubating a compound to be evaluated for use in treatment of the condition with cells which express the JMHV proteins or peptides, and determining the effect of the compound on the activity of the virus. In vitro assays in which the virus is maintained in suitable cell culture are provided as are in vivo animal models (such as a non-human primate model).

[0187] In vitro assays include infecting cells such as Japanese macaque fibroblasts, neuronal cells, peripheral blood leukocytes or susceptible B or T cell lines with the agent of interest in the presence of varying concentrations of compounds targeted against viral replication. These compounds include, but are not limited to nucleoside analogs, chain terminators, antisense oligonucleotides and random polypeptides. (Asada et al., J. Clin. Microbiol. 27:2204, 1989; Kikuta et al., Lancet 7:861, 1989). Infected cultures and their supernatants can be assayed for the total amount of virus, including the presence of the viral genome, by quantitative PCR, by dot blot assays, or by using immunologic methods. For example, a culture of susceptible cells could be infected with the JMHV in the presence of various concentrations of drug, fixed on slides after a period of days, and examined for viral antigen by indirect immunofluorescence with monoclonal antibodies to viral polypeptides. Alternatively, chemically adhered cell monolayers can be used for an infectious agent assay using indirect immunofluorescent antibody staining to search for focus reduction (Higashi, J. Clin. Microbiol. 27:2204, 1989, incorporated by reference).

[0188] As an alternative to whole cell in vitro assays, purified enzymes isolated from the JMHV can be used as targets for rational drug design to determine the effect of the potential drug on enzyme activity, such as thymidylate sunthase or DNA polymerase. A measure of enzyme activity indicates an effect on the infectious agent itself. Drug screens using herpes viral products are known and have been previously described in EP 0514830 (herpes proteases) and WO 94/04920 (U_(L) 13 gene product).

[0189] In particular embodiments, this disclosure provides an assay for screening anti-MS chemotherapeutics. Infected cells can be incubated in the presence of a chemical agent that is a potential chemotherapeutic against MS. The level of virus in the cells is then determined after several days by IFA for antigens or Southern blotting for viral genome or Northern blotting for mRNA and compared to control cells. This assay can quickly screen large numbers of chemical compounds that may be useful against MS. This disclosure also provides an assay system that is employed to identify drugs or other molecules capable of binding to the DNA molecule or proteins, either in the cytoplasm or in the nucleus, thereby inhibiting or potentiating transcriptional activity. This assay would be useful in the development of drugs that are specific against particular cellular activity, or that would potentiate such activity, in time or in level of activity. Also included are drugs identified by this assay which have an anti-viral activity, and have therapeutic value for conditions associated with JMHV infection.

[0190] Thus, an assay is provided herein for screening anti-multiple sclerosis (MS) therapeutics. Infected cells can be incubated in the presence of a chemical agent that is a potential anti-inflammatory agent or other agent of use in treating MS (such as an agent that alters the interaction of IL-2 with its receptor). The level of virus in the cells is then determined by IFA for antigens, Southern blotting for the viral genome, Northern blotting for mRNA, or PCR, and compared to control cell. This assay can quickly screen large numbers of agents that may be useful in the treatment of MS. This disclosure also provides an assay system that is employed to identify drugs or other molecules capable of binding to the DNA molecule or proteins, either in the cytoplasm or in the nucleus, thereby inhibiting or potentiating transcriptional activity. This assay would be useful in the development of drugs that are specific against particular cellular activity, or that would potentiate such activity, in time or in level of activity. Also included are drugs identified by this assay which have an anti-viral activity, and an effect against conditions associated with JMHV infection, such as MS.

[0191] Animal models are useful for resolving a number of fundamental problems of infectious diseases that include, but are not limited to, determinants of virulence of the organism, mechanisms of host resistance, mechanisms of pathogenicity, establishment and regulation of chronic infection, and antimicrobial and chemotherapeutic actions of drugs on infectious agents. Variables that are commonly manipulated to address fundamental problems include, but are not limited to, the strain of infectious agent, the infecting dose of infectious agent and the route of administration of the infectious agent, the species or subspecies of animal, the age of animal, and the genetic background of the animal (Viral pathogenesis, N. Nathanson, Lippincot-Raven, Philadelphia, Pa., 1997).

[0192] Multiple sclerosis (MS) is a chronic, debilitating inflammatory disease limited to central nervous system (CNS) white matter. Currently, there are very few effective treatments for MS. The disease may not be etiologically homogeneous, but rather a complex set of diseases that have in common pathogenic mechanisms that involve genetically predisposed individuals, and infectious agents as initiators and diverse mechanisms of inflammatory white matter destruction (Hafler, J Clin Invest 104:527-529, 1999). Genetic studies in families with MS-affected members have revealed that MS is a complex trait, that the contribution of individual genes to susceptibility is probably small, and that differences are possible between familial and sporadic forms of the disease (Kalman and Lublin, Biomed Pharmacother 53:358-370, 1999).

[0193] An animal model, including a Japanese macaque infected with a virus at least 90% identical to the nucleic acid sequence set forth as SEQ ID NO: 1 is provided herein. This animal model can be used to assess the efficacy of agents for the treatment of multiple sclerosis.

[0194] In another embodiment, in which one or more JMHV strains are employed for generating an animal model, the JMHV used may be naturally occurring variant isolates recovered from Japanese macaques and other non-human primate species, molecular clones generated from these naturally occurring variant isolates and recombinant viruses with introduced mutations, deletions or recombined genomes designed to address function of specific genes. For example, the JMHV can include a nucleic acid sequence set forth as SEQ ID NO: 1. To create the animal model, an animal, such as a non-human primate, is utilized. For example, a macaque monkey can be administered JMVH. The non-human animal is administered a JMVH by any route, including oral, inhalation, intratracheal, intravaginal, intrarectal and parenteral routes including, but not limited to intravenous, intraarterial, intradermal, subcutaneous, intramuscular, intraperitoneal and organ-specific administration routes such and intracerebral and intraocular administration. The effect of an agent can then be evaluated in the animal. The agent can be administered prior to infection with the virus, at the same time as infection with the virus, or after infection with the virus. A therapeutically effective amount of the agent is administered, and a signs, symptom, or parameter of viral infection (such as viral load or expression of a JMHV protein) is assessed. In one embodiment, the sign, symptom, or a parameter of viral infection is compared to a control, such as to an animal of the same species infected with JMHV that is not treated with the agent, is treated with a vehicle control, or is not infected with JMHV.

Pharmaceutical Compositions and Use

[0195] Pharmaceutical compositions including JMHV nucleic acid sequences, JMHV proteins, or antibodies that bind these proteins are disclosed herein.

[0196] These pharmaceutical compositions include a therapeutically effective amount of one or more JMHV polypeptide, or a nucleic acid encoding a JMHV polypeptide, or an antibody that specifically binds a JMHV polypeptide, alone or in combination, in conjunction with a pharmaceutically acceptable carrier.

[0197] Disclosed herein are substances suitable for use as vaccines for the prevention of diseases associated with JMHV infection, such as MS, and methods for administering them. Particular vaccines are directed against JMHV or related viruses, and may include antigens obtained from JMHV or its related viruses. In one embodiment, the vaccine contains attenuated JMHV, or related viruses found in humans. In another embodiment, the vaccine contains killed JMHV. In another embodiment, the vaccine contains a nucleic acid vector encoding at least one JMHV ORF, such as a surface protein of JMHV. In another embodiment, the composition contains a JMHV subunit, such as glycoprotein B, major capsid protein, or other gene products found to elicit appropriate humoral and/or cell mediated immune responses.

[0198] Various delivery systems for administering pharmaceutical compositions including JMHV proteins include encapsulation in liposomes, microparticles, microcapsules, expression by recombinant cells, receptor-mediated endocytosis (see Wu and Wu, J. Biol. Chem. 262:4429-32, 1987), and construction of a therapeutic nucleic acid (such as an anti-sense molecule) as part of a retroviral or other vector. Methods of introduction include, but are not limited to, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, and oral routes. The compounds may be administered by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, etc.) and may be administered together with other biologically active agents. Administration can be systemic or local. In addition, the pharmaceutical compositions may be introduced into the central nervous system by any suitable route, including intraventricular and intrathecal injection; intraventricular injection may be facilitated by an intraventricular catheter, for example, attached to a reservoir, such as an Ommaya reservoir.

[0199] The use of liposomes as a delivery vehicle is another delivery method of the present disclosure. The liposomes fuse with the target site and deliver the contents of the lumen intracellularly. The liposomes are maintained in contact with the target cells for a sufficient time for fusion to occur, using various means to maintain contact, such as isolation and binding agents. Liposomes may be prepared with purified proteins or peptides that mediate fusion of membranes, such as Sendai virus or influenza virus. The lipids may be any useful combination of known liposome forming lipids, including cationic lipids, such as phosphatidylcholine. Other potential lipids include neutral lipids, such as cholesterol, phosphatidyl serine, phosphatidyl glycerol, and the like. For preparing the liposomes, the procedure described by Kato et al. (J. Biol. Chem. 266:3361, 1991) may be used.

[0200] The pharmaceutical compositions or methods of treatment may be administered in combination with other therapeutic treatments, such as with additional immunosuppressive therapies.

[0201] JMHV nucleic acids can be used to generate an animal model, or to express JMHV polypeptides to produce an immune response against JMHV. In an embodiment in which one or more JMHV nucleic acids are employed for generating an animal model, or for producing an immune response, the nucleic acid can be delivered intracellularly (e.g., by expression from a nucleic acid vector or by receptor-mediated mechanisms). In a specific embodiment where the therapeutic molecule is a nucleic acid, administration may be achieved by an appropriate nucleic acid expression vector which is administered so that it becomes intracellular, e.g., by use of a retroviral vector (see U.S. Pat. No. 4,980,286), or by direct injection, or by use of microparticle bombardment (e.g., a gene gun; Biolistic, Dupont), or coating with lipids or cell-surface receptors or transfecting agents, or by administering it in linkage to a homeobox-like peptide which is known to enter the nucleus (see e.g., Joliot et al., Proc. Natl. Acad. Sci. USA 88:1864-8, 1991). Alternatively, the nucleic acid can be introduced intracellularly and incorporated within host cell DNA for expression, by homologous recombination.

[0202] The vector pCDNA, is an example of a method of introducing the foreign cDNA into a cell under the control of a strong viral promoter (CMV) to drive the expression. However, other vectors can be used. Other retroviral vectors (such as pRETRO-ON, Clontech), also use this promoter but have the advantages of entering cells without any transfection aid, integrating into the genome of target cells only when the target cell is dividing (as cancer cells do, especially during first remissions after chemotherapy) and they are regulated. It is also possible to turn on the expression of the RRV or JMHV nucleic acid by administering tetracycline when these plasmids are used. Hence these plasmids can be allowed to transfect the cells, then administer a course of tetracycline with a course of chemotherapy to achieve better cytotoxicity.

[0203] Other plasmid vectors, such as pMAM-neo (also from Clontech) or pMSG (Pharmacia) use the MMTV-LTR promoter (which can be regulated with steroids) or the SV10 late promoter (pSVL, Pharmacia) or metallothionein-responsive promoter (pBPV, Pharmacia) and other viral vectors, including retroviruses. Examples of other viral vectors include adenovirus, AAV (adeno-associated virus), recombinant HSV, poxviruses (vaccinia) and recombinant lentivirus (such as HIV). All these vectors achieve the basic goal of delivering into the target cell the cDNA sequence and control elements needed for transcription. The present disclosure includes all forms of nucleic acid delivery, including synthetic oligos, naked DNA, plasmid and viral, integrated into the genome or not.

[0204] Also contemplated are inhibitory nucleic acid therapeutics that can inhibit the activity of JMHV, for example in a subject with MS or other diseases associated with JMHV infection. Inhibitory nucleic acids may be single-stranded nucleic acids, which can specifically bind to a complementary nucleic acid sequence. By binding to the appropriate target sequence, an RNA-RNA, a DNA-DNA, or RNA-DNA duplex or triplex is formed. These nucleic acids are often termed “antisense” because they are usually complementary to the sense or coding strand of the gene, although recently approaches for use of “sense” nucleic acids have also been developed. The term “inhibitory nucleic acids” as used herein, refers to both “sense” and “antisense” nucleic acids, and includes small inhibitory RNAs.

[0205] By binding to the target nucleic acid, the inhibitory nucleic acid can inhibit the function of the target nucleic acid. This could, for example, be a result of blocking DNA transcription, processing or poly(A) addition to mRNA, DNA replication, translation, or promoting inhibitory mechanisms of the cells, such as promoting RNA degradation. Inhibitory nucleic acid methods therefore encompass a number of different approaches to altering expression of JMHV genes. Cleavage, and therefore inactivation, of the target nucleic acids may be effected by attaching a substituent to the inhibitory nucleic acid which can be activated to induce cleavage reactions. The substituent can be one that affects either chemical, or enzymatic cleavage. Alternatively, cleavage can be induced by the use of ribozymes or catalytic RNA. In this approach, the inhibitory nucleic acids would include either naturally occurring RNA (ribozymes) or synthetic nucleic acids with catalytic activity.

[0206] The inhibitory nucleic acid therapies can be used to target nucleic acids to sequences of JMHV for use in treating conditions caused by the JMHV, or proteins of the JMHV, for example for treating MS or an other immune mediated syndromes, such as an autoimmune disease.

[0207] Therapeutic, intravenous, polyclonal or monoclonal antibodies have been used as a mode of passive immunotherapy of herpesviral diseases, such as infection with CMV. Immune globulin from subjects previously infected with the JMHV and bearing a suitably high titer of antibodies against the virus can be given in combination with antiviral agents (e.g. ganciclovir), or in combination with other modes of immunotherapy that are currently being evaluated for the treatment of MS, which are targeted to modulating the immune response (such as treatment with antibodies that inhibit the interaction of IL-2 with its receptor). In one embodiment, antibodies specific for an epitope expressed on cells infected with the JMHV are utilized and can be obtained as described above.

[0208] Thus, pharmaceutical compositions which include a therapeutically effective amount of an antibody, and a pharmaceutically acceptable carrier or excipient. The antibody can be polyclonal or monoclonal.

[0209] A method is provided herein for vaccinating a subject against multiple sclerosis, comprising administering to a susceptible subject an effective amount of the peptide or polypeptide encoded by an isolated DNA molecule encoding a polypeptide or combination of polypeptides expressed by the DNA molecule, and a suitable acceptable carrier. In one embodiment, DNA is administered to the subject in an effective amount to vaccinate the subject against multiple sclerosis, or other disease associated with JMHV infection.

[0210] The vaccine can be made using synthetic peptide or recombinantly-produced polypeptide described above as antigen. Typically, a vaccine will include from about 1 to 50 micrograms of antigen, for example from about 15 to about 45 micrograms. Typically, the vaccine is formulated so that a dose includes about 0.5 milliliters. The vaccine may be administered by any route known in the art, for example parenteral, subcutaneous or intramuscular.

[0211] There are a number of strategies for amplifying an antigen's effectiveness, particularly as related to the art of vaccines. For example, cyclization of a peptide can increase the peptide's antigenic and immunogenic potency. See U.S. Pat. No. 5,001,049. More conventionally, an antigen can be conjugated to a suitable carrier, usually a protein molecule. This procedure can allow multiple copies of an antigen, such as a peptide, to be conjugated to a single larger carrier molecule. Additionally, the carrier may possess properties which facilitate transport, binding, absorption or transfer of the antigen.

[0212] For parenteral administration, such as subcutaneous injection, examples of suitable carriers are the tetanus toxoid, the diphtheria toxoid, serum albumin and lamprey, or keyhole limpet, hemocyanin because they provide the resultant conjugate with minimum genetic restriction. Conjugates including these universal carriers can function as T cell clone activators in individuals having very different gene sets. The conjugation between a peptide and a carrier can be accomplished using one of the methods known in the art. Specifically, the conjugation can use bifunctional cross-linkers as binding agents as detailed, for example, by Means and Feeney, “A recent review of protein modification techniques,” Bioconjugate Chem. 1:2-12, 1990.

[0213] Vaccines against JMHV can be made from the JMHV envelope glycoproteins. These proteins can be purified and used for vaccination (Lasky, J. Med. Virol. 31:59, 1990). MHC-binding peptides from cells infected with the human herpesvirus can be identified for vaccine candidates per the methodology of Marloes et al., Eur. J. Immunol.21:2963-2970, 1991. The JMHV antigen may be combined or mixed with various solutions and other compounds as is known in the art. For example, it may be administered in water, saline or buffered vehicles with or without various adjuvants or immunodiluting agents. Examples of such adjuvants or agents include aluminum hydroxide, aluminum phosphate, aluminum potassium sulfate (alum), beryllium sulfate, silica, kaolin, carbon, water-in-oil emulsions, oil-in-water emulsions, muramyl dipeptide, bacterial endotoxin, lipid X, Corynebacterium parvum (Propionibacterium acnes), Bordetella pertussis, polyribonucleotides, sodium alginate, lanolin, lysolecithin, vitamin A, saponin, liposomes, levamisole, DEAE-dextran, blocked copolymers or other synthetic adjuvants. Such adjuvants are available commercially from various sources, for example, Merck Adjuvant 65 (Merck and Company, Inc., Rahway, N.J.) or Freund's Incomplete Adjuvant and Complete Adjuvant (Difco Laboratories, Detroit, Mich.). Other suitable adjuvants are Amphigen (oil-in-water), Alhydrogel (aluminum hydroxide), or a mixture of Amphigen and Alhydrogel. Only aluminum is approved for human use.

[0214] The proportion of antigen and adjuvant can be varied over a broad range so long as both are present in effective amounts. For example, aluminum hydroxide can be present in an amount of about 0.5% of the vaccine mixture (Al₂O₃ basis). On a per-dose basis, the amount of the antigen can range from about 0.1 μg to about 100 μg protein per subject, for example about 1 μg to about 50 μg per dose, or about 15 μg to about 45 μg. A suitable dose size is about 0.5 ml. Accordingly, a dose for intramuscular injection, for example, would comprise 0.5 ml containing 45 μg of antigen in admixture with 0.5% aluminum hydroxide. After formulation, the vaccine may be incorporated into a sterile container which is then sealed and stored at a low temperature, for example 4° C., or it may be freeze-dried. Lyophilization permits long-term storage in a stabilized form.

[0215] The vaccines may be administered by any conventional method for the administration of vaccines including oral and parenteral (e.g., subcutaneous or intramuscular) injection. Intramuscular administration is preferred. The treatment may consist of a single dose of vaccine or a plurality of doses over a period of time. Also, the antigen could be a component of a recombinant vaccine which is adaptable for oral administration. Vaccines of the disclosure may be combined with other vaccines for other diseases to produce multivalent vaccines. A pharmaceutically effective amount of the antigen can be employed with a pharmaceutically acceptable carrier such as a protein or diluent useful for the vaccination of mammals, particularly humans. Other vaccines may be prepared according to methods well-known to those skilled in the art.

[0216] Those of skill will readily recognize that it is only necessary to expose a mammal to appropriate epitopes in order to elicit effective immunoprotection. The epitopes are typically segments of amino acids which are a small portion of the whole protein. Using recombinant genetics, it is routine to alter a natural protein's primary structure to create derivatives embracing epitopes that are identical to or substantially the same as (immunologically equivalent to) the naturally occurring epitopes. Such derivatives may include peptide fragments, amino acid substitutions, amino acid deletions and amino acid additions of the amino acid sequence for the viral polypeptides from the human herpesvirus. For example, it is known in the protein art that certain amino acid residues can be substituted with amino acids of similar size and polarity without an undue effect upon the biological activity of the protein. The human herpesvirus proteins have significant tertiary structure and the epitopes are usually conformational. Thus, modifications should generally preserve conformation to produce a protective immune response.

[0217] The disclosure is illustrated by the following non-limiting Examples.

EXAMPLES

[0218] Japanese macaque herpesvirus (JMHV) was isolated from a monkey with encephalomyelitis and the complete nucleotide sequence was determined. DNA sequence and phylogenetic analysis revealed JMHV is a gamma-2 herpesvirus. JMHV was associated with demyelinating disease in vivo. The virus can also be propagated in vitro. As disclosed herein the entire genome of a novel gamma herpesvirus, referred to as Japanese macaque herpesvirus (JMHV) has been identified and sequenced. The virus was isolated from an inflamed spinal cord lesion obtained from a Japanese macaque with spontaneous MS-like disease.

[0219] Rhesus macaques naturally harbor a virus related to KSHV, referred to as RRV, for rhesus rhadinovirus. JMHV is related to RRV, which is described in International Application No. PCT/US99/26260 filed Nov. 5, 1999, which claims priority from U.S. Provisional Application No. 60/109,409 filed Nov. 20, 1998 and U.S. Provisional Application No. 60/107,507 filed Nov. 6, 1998, are also incorporated herein by reference

Example 1 Virus Isolation

[0220] Japanese macaque encephalomyelitis (JME) is a spontaneous demyelinating disease with clinical features such as ataxia and paralysis similar to those of MS. To investigate whether a virus is associated with the development of JME, a spinal cord lesion was obtained at necropsy from a macaque with JME, dissociated and cultured with primary macaque fibroblasts. Cytopathic effects (CPE) developed in the culture after 10 days and the culture was harvested for passage. Primary macaque fibroblasts were inoculated with filtered extracts from the original culture and observed for CPE. Cultures developing CPE were harvested and analyzed by transmission electron microscopy (TEM) for the presence of virus particles. TEM examination revealed 150-200 nm virus particles with characteristic dense cores resembling herpesviruses. Limiting dilution of the original virus isolate yielded a purified herpesvirus preparation, which was subsequently expanded for viral DNA isolated and identified by degenerate PCR (Wucherpfennig and Strominger, Cell 80:695-705, 1995).

Example 2 Sequence Analysis and Identification of Open Reading Frames

[0221] Sequence analysis of the degenerate PCR product targeting the DNA polymerase gene revealed that the JMHV was closely related to rhesus macaque rhadinovirus (RRV) (Searles et al., J Virol 73:3040-53, 1999). To further identify the herpesvirus, a shotgun subclone library of the JMHV genome was generated and the genomic sequence deduced as recently described for rhesus cytomegalovirus (Hansen et al, J Virol 77:6620-36, 2003). The complete JMHV sequence was compiled and analyzed using MacVector version 7.2 (Acelrys, San Diego, Calif.). The target search criterion was for open reading frames (ORFs) that encoded proteins of 80 amino acids or more. Putative ORFs were translated and homologous proteins were identified using GenBank's BLASTP search engine. The full length nucleic acid sequence is shown in SEQ ID NO: 1.

[0222] Analysis of the JMHV DNA sequence indicated the genome is similar to all herpesviruses, has a linear, double-stranded DNA genome that is 131,217 base pairs in length and encodes 171 potential ORFs (Table 1, see also FIG. 1). The ORF finder of MacVector was used to identify all 171 putative ORFs greater than or equal to 80 amino acids. Putative ORFs were numbered by the order in which they appear in the genome. In Table 1, ORFs that read left to right are designated W, whereas ORFs that read right to left are designated by C. ORFs from RRV strain 17577 (GenBank Accession No. AF083501) were used for comparison. The complete JMHV genome sequence has been deposited in GenBank. TABLE 1 JMHV ORF Summary Position (nt) Length RRV ORF Strand From To b.p. a.a Homolog Description JM1 C 594 890 296 99 JM2 W 1444 2721 1277 426 R1 IgG receptor JM3 C 2778 3359 581 194 ORF 2 Dihydrofolate reductase JM4 W 3526 4713 1187 396 ORF 4 Complement binding protein JM5 W 5146 8544 3398 1133 ORF 6 ssDNA binding protein JM6 C 5581 5895 314 105 JM7 C 7410 7676 266 89 JM8 C 7462 7722 260 87 JM9 C 8541 8792 251 84 JM10 W 8569 10629 2060 687 ORF 7 Processing/transport protein JM11 C 10606 10929 323 108 JM12 W 10616 13102 2486 829 ORF 8 Glycoprotein B JM13 C 12565 12858 293 98 JM14 W 13219 16257 3038 1013 ORF 9 DNA polymerase JM15 C 13267 13827 560 187 JM16 C 14809 15117 308 103 JM17 W 15726 16031 305 102 JM18 W 16351 17601 1250 417 ORF 10 JM19 C 17226 17501 275 92 JM20 W 17610 18839 1229 410 ORF 11 JM21 C 19018 19641 623 208 R2 vIL-6 JM22 C 19861 20862 1001 334 ORF 70 Thymidylate synthetase JM23 C 20969 21235 266 89 JM24 C 21386 21748 362 121 R3 VMIP JM25 C 21845 22120 275 92 HHV2 RS1; collagen-like, myosin XV JM26 C 22363 22701 338 113 Myosin IA, sphingosine kinase JM27 W 22700 23008 308 103 Similar to RRV ORF RU1-R JM28 W 25392 25955 563 188 ORF 16 Bcl-2 homolog JM29 C 26062 27672 1610 537 ORF 17 Capsid protein JM30 W 27545 28444 899 300 ORF 18 JM31 W 28138 28431 293 98 JM32 C 28452 30095 1643 548 ORF 19 Tegument protein JM33 C 29590 30642 1052 351 ORF 20 JM34 W 30641 32311 1670 557 ORF 21 Thymidine kinase JM35 W 30825 31181 356 119 MHC psoriasis candidate JM36 C 30863 31111 248 83 Possible transposable element JM37 C 32279 32608 329 110 JM38 W 32298 34478 2199 727 ORF 22 Glycoprotein H JM39 C 33254 33553 299 100 Succinate dehydrogenase JM40 C 34475 35687 1212 404 ORF 23 EBV BTRF1 homolog JM41 W 34974 35285 311 104 Alpha-1A adrenergic receptor JM42 C 35301 35687 386 129 ORF 23 EBV BTRF1 homolog JM43 C 35737 37938 2201 734 ORF 24 EBV BcRF1 homolog JM44 C 37346 37612 266 89 JM45 W 37937 42073 4136 1379 ORF 25 Major capsid protein JM46 W 39498 39821 323 108 JM47 C 39842 40282 440 147 JM48 W 40188 40439 251 84 ICHIT protein; mucin JM49 W 42105 43022 917 306 ORF 26 Minor capsid protein JM50 W 43047 43871 824 275 ORF 27 EBV BDLF2 homolog JM51 W 44035 44310 275 92 ORF 28 JM52 C 44360 45406 1371 349 ORF 29b Packaging protein (spliced) JM53 W 45720 46373 653 218 ORF 31 EBV BDLF4 homolog JM54 C 45836 46195 359 120 Collagen family member; ataxin 7 JM55 W 46310 47695 1385 462 ORF 32 EBV BGLF1 homolog JM56 W 47676 48686 1010 337 ORF 33 EBV BGLF2 homolog JM57 C 47768 48136 368 123 Calcium channel JM58 C 48218 48607 389 130 Protein kinase-like JM59 C 48604 49587 983 328 ORF 29a Packaging protein (spliced) JM60 C 49010 49276 266 89 JM61 W 49586 50572 986 329 ORF 34 EBV BGLF3 JM62 C 50504 50950 446 149 JM63 W 50553 51002 449 150 ORF 35 EBV BGLF3.5 homolog JM64 W 50908 52215 1307 436 ORF 36 Kinase JM65 W 52196 53638 1442 481 ORF 37 Alkaline exonuclease JM66 C 53882 55018 1136 379 ORF 39 Glycoprotein M JM67 W 54536 54850 314 105 Histidyl-tRNA synthetase, ligase JM68 W 55153 57156 2003 668 ORF 40 Helicase/primase complex component JM69 C 56124 56474 350 117 Unknown JM70 C 57153 57968 815 272 ORF 42 EBV BBRF2 homolog JM71 W 57325 57573 248 83 Chromatin associated protein JM72 C 57907 59652 1745 582 ORF 43 Capsid protein JM73 W 59591 61963 2372 791 ORF 44 Helicase/primase complex component JM74 C 61249 61662 413 138 Transcription factor AFX1, ChCMV UL7 JM75 C 62004 63065 1061 354 ORF 45 EBV BKRF4 JM76 W 62823 63086 263 88 Plexin JM77 C 63107 63874 767 256 ORF 46 Uracil DNA glucosidase JM78 C 63850 64341 491 164 ORF 47 Glycoprotein L JM79 C 64600 65769 1169 390 ORF 48 EBV BRRF2 homolog JM80 W 65629 65880 251 84 NADH-ubiquinone dehydrogenase chain 8 JM81 W 65963 66208 245 82 JM82 C 66000 66905 905 302 ORF 49 EBV BRRF1 homolog JM83 W 66058 66315 257 86 JM84 W 67096 68640 1544 515 ORF 50 Transactivator JM85 C 67920 68594 674 225 Chromatin remodeling complex JM86 W 68957 69469 512 171 BZIP transcription factor JM87 W 70026 70760 734 245 Glycoprotein R8.1; mucin JM88 C 70328 70606 278 93 Neurexin 1-alpha JM89 C 71001 71420 419 124 ORF 52 EBV BLRF2 homolog JM90 C 71483 71797 314 105 ORF 53 EBV BLRF1 homolog JM91 W 71873 72745 872 291 ORF 54 DUTPase JM92 W 72520 72942 422 141 Transducin-like enhancer JM93 C 72806 73438 632 211 ORF 55 EBV BSRF1 homolog JM94 W 73420 75936 2516 839 ORF 56 DNA replication protein JM95 C 75447 75722 275 92 Cytochrome oxidase subunit I JM96 W 76035 76304 269 90 JM97 W 76162 77484 1322 441 ORF 57 Immediate-early protein JM98 C 77857 79098 1241 414 R6 VIRF JM99 W 78411 78656 245 82 JM100 W 79163 79579 416 139 Ribonuclease III JM101 C 79269 80510 1241 414 R7 VIRF JM102 W 79521 79769 248 83 Hepatitis B core protein JM103 C 80836 81891 1055 352 R8 VIRF JM104 C 82068 83153 1085 362 R9 VIRF JM105 W 82206 82613 407 136 RNA polymerase associated factor JM106 C 83628 84785 1157 386 R10 VIRF JM107 W 84837 85082 245 82 Transposase JM108 C 84932 86104 1172 391 R11 VIRF JM109 W 85290 85550 260 87 JM110 W 85968 86243 275 92 JM111 C 86479 87546 1067 356 R12 VIRF JM112 C 87707 88801 1094 365 R13 VIRF JM113 C 87763 88023 260 87 JM114 C 88087 88395 308 103 JM115 C 89047 90129 1082 361 ORF 58 JM116 C 90140 91324 1184 395 ORF 59 DNA replication protein JM117 W 91017 91259 242 81 JM118 C 91455 92399 944 315 ORF 60 Small ribonucleotide reductase JM119 C 92381 94747 2366 789 ORF 61 Large ribonucleotide reductase JM120 C 92929 93345 416 139 JM121 W 94175 94468 293 98 DNA repair and genetic recombination JM122 C 94751 95746 995 332 ORF 62 Assembly/DNA maturation protein JM123 W 95745 98564 2819 940 ORF 63 Tegument protein JM124 W 98568 104468 5900 1967 ORF 64 Tegument protein JM125 C 99388 99753 365 122 JM126 C 99611 100054 443 148 Drug resistance protein JM127 C 101108 101428 320 107 JM128 C 102290 102568 278 93 JM129 C 102857 103150 293 98 JM130 C 104302 104643 341 114 JM131 W 104555 105856 1301 434 ORF 64 Tegument protein JM132 C 105581 106003 422 141 C-myc promoter binding protein JM133 C 106220 106729 509 170 ORF 65 Capsid protein JM134 W 106299 106559 260 87 JM135 C 106733 108079 1346 449 ORF 66 EBV BFRF2 homolog JM136 W 107289 107696 407 136 JM137 C 107974 108780 806 269 ORF 67 Tegument protein JM138 W 108002 108316 314 105 JM139 C 108796 109056 260 87 ORF 67.5 JM140 W 109190 110563 1373 458 ORF 68 Glycoprotein JM141 C 109783 110166 383 128 JM142 C 110578 110904 326 109 Aldehyde dehydrogenase JM143 W 110585 111478 893 298 ORF 69 EBV BFLF2 homolog JM144 W 112447 112698 251 84 RRV ORF RU3-R JM145 W 113610 114479 869 290 RRV ORF RU4-R JM146 C 114427 114753 326 109 JM147 C 115214 115918 704 235 RRV ORF RU13-L; serotonin receptor JM148 W 115671 115928 257 86 EBV nuclear antigen JM149 C 115717 115983 266 89 JM150 W 116366 116650 284 95 Lagopus leucurus gag polyprotein JM151 C 116918 117442 524 175 ORF 71 FLIP homolog JM152 C 117501 118265 764 255 ORF 72 Cyclin D homolog JM153 C 118608 119918 1310 437 ORF 73 Latency-associated nuclear antigen JM154 W 119237 119617 380 127 JM155 W 119614 119940 326 109 JM156 C 119824 120075 251 84 JM157 W 120484 120744 260 87 JM158 W 120572 121333 761 254 R15 N-CAM Ox-2 homolog JM159 C 120689 121186 497 166 CD36; carotenoid uptake JM160 W 121628 122656 1028 343 ORF 74 IL-8 receptor; G protein coupled receptor JM161 C 122762 126658 3896 1299 ORF 75 Tegument protein JM162 C 123126 123398 272 91 JM163 W 123423 123577 154 85 JM164 W 123810 124133 323 108 JM165 W 124395 124790 395 132 K1 glycoprotein HHV-8 JM166 C 124683 125165 482 161 Collagen family member JM167 W 126063 126371 308 103 Myosin phosphatase JM168 C 128122 128493 371 124 C-C Chemokine receptor JM169 C 128789 129046 257 86 JM170 C 129970 130404 434 145 Unknown JM171 W 130383 130655 272 91

[0223] The overall G+C content was 51.9% and is distributed evenly throughout the length of the genome. The genes were named from left to right starting at the first ORF on the coding or complementary strand (e.g., 155). The JM prefix precedes each numbered gene to distinguish different viruses' nomenclature (e.g., JM1). The arrangement of JMHV genes is shown in FIG. 1 and was compared with other primate gamma-2 herpesvirus genomes. A phylogenetic analysis was performed using six ORFs from HSV-1, Kaposi's sarcoma-associated herpesvirus (KSHV), human cytomegalovirus (HCMV) and JMHV. The DNA polymerase, helicase, glycoprotein B, major capsid protein, single-stranded DNA binding protein, and uracil N-glycosylase were examined by bootstrap analysis with the maximum parsimony method. Alignments were performed using ClustalW. The KSHV proteins were used as the root for analysis. The phylogenetic analysis revealed that JMHV is a gamma-herpesvirus most closely related to RRV.

[0224] JMHV ORFs are arranged collinearly with other gamma-herpesviruses, including RRV and KSHV (Chang et al., Science 266:1865-9, 1994; Moore et al., J Virol 70:549-58, 1996; Russo et al., Proc Natl Acad Sci USA 93:14862-7, 1996; Searles et al., J Virol 73:3040-53, 1999). Most all of the conserved herpesvirus gene blocks are retained in JMHV in both position and orientation, coding all of the necessary enzymes and structural components. Of the 171 ORFs, 81 (47%) are homologous to known RRV proteins. However, the homologous genes are on average 88% identical with a high of 99% and a low of 36%. A protein/protein comparison was done. The percent identity of the two proteins and the scores (except value; calculated based on the size of nr database) for the alignments are shown in Table 2. TABLE 2 Similarity between JMHV genes with amino acid sequence homology to RRV Score JMHV Length RRV Homolog Identity for (except gene (aa) homolog length (aa) overlap (%) value) JM2 426 R1 424 82 1845 JM3 194 ORF2 189 94 937 JM4 396 ORF4 646 51 1001 JM5 1133 ORF6 1133 97 5878 JM10 687 ORF7 687 90 3240 JM12 829 ORF8 830 89 3789 JM14 1013 ORF9 1015 93 4982 JM18 417 ORF10 417 91 1997 JM20 410 ORF11 410 97 2128 JM21 208 R2 208 85 915 JM22 334 ORF70 334 93 1637 JM24 121 R3 116 65 378 JM28 188 ORF16 188 76 734 JM29 537 ORF17 537 82 2211 JM30 300 ORF18 300 95 1527 JM32 548 ORF19 548 97 2796 JM33 351 ORF20 351 91 1700 JM34 557 ORF21 558 87 2532 JM38 727 ORF22 705 73 2638 JM43 734 ORF24 733 90 3477 JM45 1379 ORF25 1379 97 7077 JM49 306 ORF26 306 99 1556 JM50 275 ORF27 270 90 1327 JM51 92 ORF28 92 91 459 JM52 349 ORF29B 349 94 1689 JM53 218 ORF31 218 90 1068 JM55 462 ORF32 465 91 2255 JM56 337 ORF33 337 91 1630 JM61 329 ORF34 329 92 1612 JM63 150 ORF35 150 94 702 JM64 436 ORF36 436 93 2196 JM65 481 ORF37 481 96 2496 JM66 379 ORF39 379 94 1844 JM68 668 ORF40 469 96 2399 JM70 272 ORF42 273 95 1376 JM72 582 ORF43 577 95 2810 JM73 791 ORF44 791 98 4092 JM75 354 ORF45 353 68 1227 JM77 256 ORF46 256 87 1226 JM78 164 ORF47 170 55 440 JM79 390 ORF48 390 92 1759 JM82 302 ORF49 302 99 1595 JM84 515 ORF50 515 92 2492 JM89 124 ORF52 124 79 532 JM90 105 ORF53 105 59 300 JM91 291 ORF54 291 97 1479 JM93 211 ORF55 211 99 1092 JM94 839 ORF56 829 95 4186 JM97 441 ORF57 443 83 1890 JM98 414 R6 416 81 1778 JM101 414 R7 416 90 1978 JM103 352 R8 352 92 1752 JM104 362 R9 254 89 1217 JM106 386 R10 386 86 1814 JM108 391 R11 391 77 1617 JM111 356 R12 356 88 1739 JM112 365 R13 365 84 1697 JM115 361 ORF58 361 74 1319 JM116 395 ORF59 395 94 1937 JM118 315 ORF60 315 98 1589 JM119 789 ORF61 789 96 4008 JM122 332 ORF62 332 98 1696 JM123 940 ORF63 940 92 4506 JM124 1967 ORF64 2549 92 9299 JM133 170 ORF65 170 66 557 JM135 449 ORF66 449 92 2212 JM137 269 ORF67 225 97 1120 JM139 87 ORF67.5 87 95 431 JM140 458 ORF68 458 94 2361 JM143 298 ORF69 298 97 1520 JM151 175 ORF71 175 91 836 JM152 255 ORF72 255 76 967 JM153 437 ORF73 449 36 162 JM158 254 R15 254 88 1190 JM160 343 ORF74 343 78 1387 JM161 1299 ORF75 1299 90 6241

[0225] Unique to JMHV are numerous small ORFs that have low homology to enzymes or structural components found in nervous tissue. Many of these putative proteins are less than 100 amino acids, which is less than what was reported in the characterization of RRV (Searles et al., supra). These potential ORFs are unique to JMHV, as analysis of the RRV genome for ORFs encoding proteins of 80 amino acids or more failed to identify similar ORFs. From this analysis it was determined that these small ORFs are specific to JMHV and includes proteins such as myosin XV (JM25), myosin IA (JM26), ataxin 7 (JM54), chromatin associated protein (JM71), chromatin remodeling complex (JM85) and Neurexin 1-alpha (JM88) (Del-Favero et al., Hum Mol Genet 7:177-86, 1998; Liang et al., Genomics 61:243-58, 1999; Patzke and Emsberger, Mol Cell Neurosci 15:561-72, 2000). Thus, these proteins could be involved with molecular mimicry or epitope spread leading to the MS-like disease observed in the Japanese macaque.

[0226] The sequence of the JMHV ORFs are provided in Table 3. TABLE 3 ORF sequences JMHV SEQUENCE ORF SEQUENCE IDENTIFIER JM 1 MRWAWFSPFLSHQLGVSNHAPSPGPTSAPLPIPLLPVPSPASMLPAP SEQ ID NO: 2 TALSVRSPRATCRADLGRLPGGPGEGSGPVSSCGPATPSHAAGRLPH YYQP JM 2 MFVLLIFILLQPASLELLPAKLTAVPTWCPPHPGDTYLLTCRGTSTA SEQ ID NO: 3 RDQRSTQWFRNNTLMHGSNFYGRLVSVTPNSTISDWYACQTKTTTRS NSIDFRVRSSRLTLQERCSSYGYSNANNTRVLRCYSGGNVTLRNVVF HLNGTAVINGTTTDIYTFVLTEKTGGTYYCSAFIGTEKLYSQKINVF FTSFTFKHTDNVQMGSEFNKTEQIQQTANVQHTANYVVFSVPVFSIG VLTGIAISLIMCWLFTLRCNKNSESSNNRHAHQTSYIQPSHNQHSHT SESTTHTYRNDHQEESIEELPNQHTRKTNSCQTVLLEVKNVAFDGPQ GNLHNTNDEVMEQYDDVVVENIEQTSYDNNIEQMDYSDIIRPNFNYY SGLILEEVDEVFYNELANQYHGLILENLDHDEYNHLNKLNMIEQYDW LE JM 3 MDITVNCIVAVDKQLGIGKNGTMPWPYLKNEMMYFQKMTSTPSVIGE SEQ ID NO: 4 KNVVIMGKRTWFSIPEKKRPLANRINIILSRELREPPKGAHFLARTL DDAFNFYRQYKLTKQLNTVWVIGGKSVYESVLNYECSLKLYITRIME SFDCDVFFPSINFTEYTMLSELPGKDTNFEENGIKYKFQVYEKRLIN KAVTQ JM 4 MRLIMFWFPVTVCFVCHFILVNAQNETNVTCDKPNFDRFMVAMEKKE SEQ ID NO: 5 KYVLGDKVELTCRPGYTLQGKVYVQCLQSGMWTTPNAECHRKKCTNY GDILNGQVIVPDSDNAFKFGTNITYKCNTGYLLLGSMVRTCLLTGNS NTVNWQPAAPTCEIEKCKKQPDIENGKYYPVQDFYNYLETITFTCNK DFSLIGMTTTTCMTMGTWSSPVPKCEQITCSAPNIEHGTLLVGSSRV YKHGQSITIGCENGFTLNGHKMCTCEYSSWNPPLPTCVPINKTVPTP SEVPSPGTNKQERPTPENPKSHESETTTETPKTGTHKSETPSKKIPN PETHKPTTPKSGTSEQTTNRPSKAPSQNPPMEPPMSKWKRHVVLVLF ASVASLLFVLVTLYCCFLK JM 5 MASKGNAGQPLEDNQGSRAPIGACGYVYAYSKQDFPFAEASILGNRP SEQ ID NO: 6 SGSGVFSLPILYGLTVEHEFPLTVKAAHKKVDTTTLAVKVTCFHREV IVFHNANLFRPVFEGTGLNELCEEARALFGYTQFIEPGPPHGIWNPL ECPQLPDKDEMFLGVVVTEGFKERLWRGCLVPAVFQTQQVQIAGRQA FKVPLYDEDLFAPHGHRMPRFYHKDVSAYLYNSLFTSIAQALRLKDV TAVIHATEKQFMQDHYKIAKIVQAKQFSTTLPKTADGSSHMTVDSVV AELALSYGCMFLECPQDACELLNYDSWPIFDGCDSSEDRVNALERWS AEQAVHVAGQLFAANSVLYLTRVQKQAPRGQKGDVNVYNSFFLQHGL GFLNEATIKENGSEAFKGVPSNALDGSSFTPYHLAYAASFSPHLLAK LCYYMQFLQHHKSSTNQTFNIVHYVGTAANSEMCTLCHGDTPGTCLN TLFYRLKDRFPAVTTPQRRDPYVVTGTAGTFNDLEILGNFASFRDRE EDGNPADEHPKYTYWQLCQTVTEKLSAIGITEDQDNHVNLITNIQSF LRVFKGIDSVVDGEVMKFINSMIKNNFNFREHVKSVHHILQFCCNVY WQAPCAVFLNLYYKSLLWIIQDICLPYCMIYEQDNPAMGILPSEWLK MHFQTLWTNFKAACLDRGVLTGCELKIVHRDMFCDFFDTDAGSNGLL APFKMQVRIARAMMVVPKSIKIKNRIIFSNTAGSEAVQSGFVKPTGT RDTYVVAGPYMKFLNSLHRALFPNTKTAALYLWHKISQTNKTPVLKD VPDDELAELVSYVKTNSLAFEETNVLDVVPDSLMSYARIKLNGAILR ACGQIQFYATTLHCLTPVLQTIDAEEYPHVLGSAAIATPVAYLSEIR GRTALTVQTTARQPVAATGRLRPVITVPMVVNKYTGVNGNNNVFHCG NLGYFAGRGVDRNLWPESSPFKKTGVSAMLRKRHVMMTPIVDRLIKR AAGQTISTFEAESVKRSVQALLEDKDNPNLLKSVILELIRHLGKGCQ DLSSEDVQYYLGDYCMLTDEVLFTLDNIAQSGVPWTFEDAGALIEDR QNTDDLQFVDSDDIATASCQPPEEQLPTPSAGALLAGKKRKINVLLS DLDL JM 6 MVLHELFFCGVDDRRHVFESQGLGDTGKKGVVEVRANVFMVKPRHPM SEQ ID NO: 7 PVRCEQVFVVQRHFERLTPGDLHLLGLKHCGNETAPPQSLLKPFRHD NAKEHLILVR JM 7 MAPFSLILAYDMRESGTTSSTFVSSNARLLVLTYDTSSASSSSGTSF SEQ ID NO: 8 RTGVLLVWEILCHRYSAAVLVFGNSARWSEFRNFMYGPATT JM 8 MQRCGVELNLTARPQNGPVQFNPRVRHEGIRDHVQHVRFLEREAVGF SEQ ID NO: 9 DVRHQLRQLVVRDVFQDWGFVGLGDFVPQVQRGGLGVWE JM 9 MFLARCSTSSDRLDVSTEFCLRSSGRRSRFRFSICVFVFRMREPSIL SEQ ID NO: 10 RGSAKTTRLRSTARADSCAYKAASSLAIVVRRPRFS JM 10 MARELAALYAQLSALAVDLSLVVFADPRSIDGSRILKTKTQIENLNR SEQ ID NO: 11 DLLPLLRKQNSVETSSLSLEVEHLAKNIEDKLGELERSLRQRYSSRE HFETLHLRPECHYHATVTFEFYGGGLIDVNMCLINDVELLCKRLGSV FYCIGANEALSGLDRVLAFLSTLRGISPIPHPDLYVTSVPCVQCLRE IELVPNQGSSLLAVLADRHCDHLCKKVRAEPIHGLFETELSQLGLKV AKGSDATQHGVRSSADQLRESSLAAIQDHNIFKRVSASIMELSNLIY WNAGQTGLQTGTENECSQMAKLLTHEAEMHEHRALITPKQSAAHFYD CFRPDPIESLFCGGLFNSIDDTINALSRDCSVTFFQQANYTNVMRKQ NELFTRLNSILCQGSAGSQKPATPSEPRTATVAATAASDVIKDAQYR KEQYMKKVARDGFKKLTECLQTQSAVLANALCMRVWGGVAYGEASEL VNHFLLRRRFVALPWEARCRSNQILFENSKYIKNSLYSQRLSREHVE IITLQFYGLITGPLTRQSDLFPGPANVVLAQCFEAAGMLPHHKMLVS EMIWPQIQPKDWIDQTFNRFYQLPEGDLNAVQKSAWCFIRELVLSVA LYNRTWEKTLRIFSLAREKPSISDLDVKSLTPGLYLTYEQNTPLVLI SQMTGWIFKDLYALLYHHLQLSDGHDDN JM 11 MWGTIFFLNTIRMPSWCVLSSVPGHVFSRLNLKSSPVAEALHTRNLN SEQ ID NO: 12 ASALGGFSGGVGVDGPGVDFAVVVTPFGVVTFSPTAAPIAIITTHAR SRRRVRLVIIMAV JM 12 MMITNRTRRLLRAWVVIIAIGAAVGENVTTPKGVTTTAKSTPGPSTP SEQ ID NO: 13 TPPENPPRAEAFKFRVCSASATGELFRFNLEKTCPGTEDKTHQEGIL MVFKKNIVPHIFKVRRYRKVATSVTVYRGWTETAVTGKQEVIRPVPQ YEINHMDTTYQCFSSMRVNVNGIENTYTDRDFTNQTVFLQPVEGLTD NIQRYFSQPVLYTTPGWFPGIYRVRTTVNCEIVDMIARSAEPYSYFV TALGDTVEVSPFCLNDSTCSVADKAENGLGVRVLTNYTIVDFATRTP TTETRVFADSGEYTVSWKAEDPKSAVCALTLWKTFPRAIQTTHEASY HFVANDVTATFTSPLSEVANFTGTYSCLDNVIQKTLNATIKKLSDTH AANGSAQYYETEGGLFLLWQPLTQLSLVDEMRGLNDTTPAPPTTSTA SRVRRSVDTNSQTAEDLAAPQLQFAYDKLRASINKVLEELSRAWCRE QVRDTYMWYELSKINPTSVMTAIYGRPVSAKFVGDAISVTDCVTVDQ GSVSIHKSLRTSTPGICYSRPPVTFRFLNSTTLFKGQLGPRNEIILT DNQVEACKETCEHYFIASNVTYYYKDYVFVKKINTSEISTLGTFIAL NLSFIENIDFRVIELYSRAEKKLSGSVFDIETMFREYNYYTQRLAGL REDLDNTIDLNRDRLARDLSDIVADLGDVGRTVVNVASSVITLFGSI VSGFINFIKSPFGGMLMILVIVAVILIVFALNRRTNAIAQAPIRMIY PDIDKMQPSGGKVDQEQIKNILAGMHQLQQEERRRLDEKQRSAPSLF RPASDGLKRRFRGYKPLENEEAQEYEMNK JM 13 MGAWAMALVRRFSANTIRMTATITRIMSMPPNGLFIKLMNPLTIDPN SEQ ID NO: 14 RVITLLATLTTVRPTSPRSATISDRSRARRSRFRSIVLSRSSRSPAS RCV JM 14 MDFFNPYLGPRGPRPPSHKCTDAPAPAGAVQPPPDVCRLIPACLRTP SEQ ID NO: 15 GAGGMIPVTIPFPPTYFENGARGDVLLAHERSMWTARGQRPVVPDPQ DQSITFHAYDVVETTYAADRCAEVPSRFQTDIIPSGTVLKLLGRTEN GTSVCVNVFRQQVYFYAKVPAGVNVTHVLQQALKNTAGRAACGFSTR RVTKKILKTYDVAEHPVTEITLSSGSMLSTLSDRLVACGCEVFESNV DAVRRFVLDHGFTTFGWYSCAPATPRLAARDARTALEFDCSWEDLSV QADRSDWPPYRIVAFDIECMGEAGFPCATRDGDAVIQISCVFYTTRE GAPNPPNILFSVGTCDPIPDTDVLEFPSEYDMLVSFFAMLRDFEVDF LTGYNISNFDLPYLITRASQVYNLRLNEYTKIKTGSIFEVHEPRGGG GGFMRSVSKIKIAGIVPIDMYQVCREKLSLSDYKLDTVARQCLGGKK EDVSYKDIPPLFRSGPGGRAKVGSYCVMDSVLVMDLLKMFMIHVEIS EIAKLAKIQARRVLTDGQQLRVFSCLLEAAARDNFILPVPTPEGQGG YQGATVINPIPGFYDEPVLVVDFASLYPSIIQAHNLCYSTMIHGRDL HLHPNLTPDDYETFVLSGGPVHFVKKHKRESLLGRLLTVWLEKRRAI RRTLAACDDPSLKTILDKQQLAIKVTCNAVYGFTGVASGLLPCINIA ETVTLRGRTMLEMSKSYVEALTTDNLRTRLGREVTACHGARFRVVYG DTDSLFIACDGYSAEAVSAFCDDLAARITADLFPPPIKLEAEKTFKC LLLLTKKRYIGVLLNDKMVMKGVDLIRKTACKFVQERCRSILDLVLH NQEVKAAARLLCKRPPHAVYEEGLPAGFIKIVEVLNASYVDLRNSVV PIEQLTFSTELSRPVCDYKTTNLPHLAVYQKLASRCEELPQVHDRIP YVFVDAPGALKSDLAEHPDYVKQHQIPVAVDLYFDKLVHGAANILQC LFGNNADTTVAILYNFLNVPYKLFS JM 15 MLRDVVRFENFFGYSSGREAARGPAGGVLEGLLEDVGDVDAGWDLRV SEQ ID NO: 16 EIYLLTEHVHAHAGAVLGSPQELEHGSARNNVRLEAARYLGAPVRRV RRFNDVVRVKRNGLVLGVRDDWPLAARRPHGPFVGEQHVSARAVFKV RRRERDRDRDHPACPRRSEAGGNEPADVWWRLISTGAGGGGRIGAFV JM 16 MHRSAAQHERLVVVRRQVGVQVQVSSVYHGGVAQVVRLDDAWVQAGK SEQ ID NO: 17 IDHQDRLVVKPRDGVNTHRRALITPLSLGRWDREDKVIPGRGLQQAGE HAKLLAVR JM 17 MPLHPGPGAPQSGGQGGGAAVVQATAARGIRGGVAGGLYKNCGGPQR SEQ ID NO: 18 ELCGPSKQRRAHRAVNVLDRAQPPRLRLQDHQPAPPGGVPEAGEQVR GAAPGAR JM 18 MLVNELSMVLGDWEVTFHRGKFSFVNLARLQTFKGHGGYAKIRLPFS SEQ ID NO: 19 LDQLLHQHFAFGLVTRLNELPPFSDCVALIAPRDSGGDADAARVAPG FVLDSSRPLTVWVNANGRHTVRFCLLFLKPIDLERAVTYVFGENGGA RSEGAPKPTCNTESLPGGPLRVSGEASQTSPHSFVAYFPTADPVACL SLLRLQVRPFSDDAAHRDARISPKYVTFSNAGGNVCKASVHTLSPSR CKTAQMEIIYAPGDPNAEIVLGQSGPVLPTHTGGRVLGVYADAEKTI QPGSSAEVRVQLIFQQGAAARGDLAFLVAGVAPEPLFIVTPTLLLSG CTTHLRLFNPNGTPTTIKRDTLVAAAAPCPVVRVSSADDAPRDLVAS PDTGALSIDAFTIPVGLPGVVSAECHVSMRDNGVHERMSH JM 19 MESAPVSGDATRSRGASSAELTRTTGQGAAAATRVSLFIVVGVPLGL SEQ ID NO: 20 NRRRCVVQPESKSVGVTMNRGSGATPATRNARSPRAAAPCWKIN JM 20 MGTPVRFFRGEWQTSSLVDNGTPRYSSLVWAATIHDGYLTLVNRSEL SEQ ID NO: 21 CVTERSPCLPACPSIGRLVGKRFPGFAFASATLGDRGTRTVFYAFGH RDNPLDIVPAVVERADRELVLRVHAPRTTRVSRYGLKIFVAIVTVVR PPGVFLHFPQDRVPIALTDACSQEGSRLTSEEPWIKIQGFPVLSDET AHPFLLTQKTKPFTERKFCRLIMDDNQLSAVNTVYLGKQHVRVTVTR PPETIVTDGPVTATLSLTGNAPIAFRHNPYFELPWSSTTAIFTPVVY VGLTVCIPPNCSKFVRYGNTYVSAFNRKLTAIISNHAHDGGFRIQDC EWPPNREIEILVTNVTQAPVYVSTGTQLGRAIFVFAPRFGGPAKLRQ LLGHRSRALELPGGVTVDSQKLCRFETMYLFST JM 21 MFPVWFVLFYLSCWAASPTLAPPPTAAGINVLPQWAGNRASLDRTRG SEQ ID NO: 22 RLSELGLNIQRWFVYLCYHSTLCRVREYPRIMSFINFPILMSNVECQ RREFRGAECMNAMVRGLRAYESYLTRSKMLLDDAPGNAGAAAIGSAV TVVLSALNSLIEELPVDNKIGGVESNDKIVPALAEQSPGDVILSAFR LLEYLQMFLRDGRRAIAMM JM 22 MIVLVHLGICYVKKIIPACLSGIAAVRCRVSRGSEVAAARAPDGRGE SEQ ID NO: 23 HGELQYLAHLDLIIRHGVQRDDRTGVGTRSVFGLQARYNLRDEFPLL TTKRVFWRGVVEELLWFIRGSTDSTELSRRGVKIWDAHGSRAFLAAQ GFGDRREGDLGPVYGFQWRHFGAEYRGADADYEGQGVDQLRYVVDLI VRRPHDRRIVMCAWNPADLARMALPPCHVLCQFYVARGELSCQLYQR SADMGLGVPFNIASYALLTYLIAHVTGLTPGDFVHTLGDAHVYNNHV GPLLLQLGRTPRPFPRLKILRKVTRLEDFTRADLSLEGYDPHPHIEM EMAV JM 23 MCLHGGASTMTLKINVFCGSCTMRVWLMNAGGDSGGDAGGDSGGDAG SEQ ID NO: 24 GDSGGDAGGDSGGDAGGDSGGDAGGDSGGDAGEGPRGFTTR JM 24 MRVLVIGAFFAVFACVVDYAFPMGSMSGPAPEVCCLGYINKLPPSGA SEQ ID NO: 25 VALYYYTSSQCTLDAVILETHRGQKLCANPGDDGVRKLLQKVDNRPK RNKGRRTRRSLLDDASDEGLESGSGF JM 25 MRRVCLGGGDFPFIAGTGPLLVLEIPFSTGSLLRRKAVYLFGESPFF SEQ ID NO: 26 RTPGATVVRHARFGTRDATSGREARAPGGWPRLVSVEADPGRGY JM 26 MLFLVAIGDIFRCPPNDPVRRGFFGSFGGHRKMFPRARRATVETIFS SEQ ID NO: 27 DPLVTPEPAPPRGAPCLGAEQSVLVRTPNAGLAVPTPARKTRGTPAG FYAITLCYFGVGAPRCPC JM 27 MSGVSVTRGAEAAGGGVGKNSGRRARVSVMTRLDGGHLAAGQRREHR SEQ ID NO: 28 ERPAGGAARDRAPRSVKMADRRRRLGAADVNHGGEERRWSGYTSITE GRAGWQII JM 28 MAAIQGPPPLPEEENENSLPDDVYAIEGIFLYCGLGQAEYLHHPVFS SEQ ID NO: 29 PIKEFISSFLKDSARLYERLLRHTDYRSLRGLNAIGQGMLHINTDGR HNWGRALAVLGLGAYVVDKIRDDERLLTFAIAVLPVYAYEALESQWF RSHGGWEGLRNYCERILRHRRNARRHMCYGVAAGLLALVALFAIRR JM 29 MTSVYVGGYVDVVSLPKIEKDLYLEPSIVATLLPYTNPLPINIEHVP SEQ ID NO: 30 EAHVGHTLGLFQVTHGIFCLGKLTSPDFLALASRLAGDSRAAQIQLN PMPRDPLLEMLHTWLPELSLSSLHPEELQDPNHPPAFQHVSLCALGR RRGSIAVYGPDPTWVVSKFDSLTRDEAGKITSKCLDLCERQVTPPEF AAPLETLMAKAIDAGFIRDRTDLLKTDKGVARVARSTYLKASQSPSS QHGGNRDTQTMSALPDDNITIPKSTFLTMVQSSLDHMRNQGQRAYVS APPSMPATAAYPSWIPPPELTVPSYAPPVAPPFPFQSAFAPQPSPYA ATYYSPTYGYAQAPSRHQKRKRDVELSDEPVFPGEEVGIHKDVMALS KNILDIQADLRDLKRAASQTSGEKDTDQRPQPPPVQFSWPQTYASAP YLAYQPQWYPGTDTHLHASQPYQIAQGIQQTQPPPPQPASHHAGLAT QPVAPAPAAQESANSNAVPSASAPRAGACPPLDSDCGQSARAPVEAS VQPAPVSQIQKMFCEELLK JM 30 MFIGRGFVYGSRVATIEGSKYRSFSIFGRLTTSTYPPTYTEVMLGRC SEQ ID NO: 31 LREPKEMSAGLRGLMWRVIRCENLNTFLPGELRFLHLVLCEMYNYGL NVYLLKEAIANTGTRDDIVLGRKVPVEFWKIIYDGLREMGVSDATLL SETKRGALWLYFNGRPCLLKGLGDYVFCRLGLSHSVRVVPENLTDGN YLYNLGSVIPCRLLVALSYCLAFWGHADHEPWVRLFAGKIFILYLII SGHIMPRKSILEQVGTSGYGGFVEAVCRDVRAVHGIPAWDFAAAAPA LTSRQTDYLFAFNNSVV JM 31 MSPASGAELLLGVLGARRPRALGQVVRRQDFYTVLNNIRPHYATKVN SEQ ID NO: 32 LRTGGNVRVRWLCRGCVSRRSRGPRHSGVGFCGSGSGVNVSTDGLPV CVQ JM 32 MRTSEKCCMRYPRKPARQITATFWAPHPNNVLFIHKPSLIEERRNAF SEQ ID NO: 33 VMRNQQLALRVHTLRKNLLRLELDNVLQTHQRETEMVMRDLDTIQNM VGDLRSPTRETADTQTSINPRPKIAPQTHGDAFVVTIAPGDPGFTVN QDLRLELLPSLYMNQNQWLPQYGPWYSSLTDNAMQRRVFPRDLRGTT NFQNSTSLKLMSAVISTAASITQDFYADVRNVSDTQAALCLLNGYYC HRTGTPLPPTRDGLWDNLGTKLATLISHLKQNTKGLGFEFTYSNPKQ RASLAPLNKETKYSADFFTNHVIYATLAQSGLLPGSKNPGTGQPPGP DLVYILATTLFSEDVPPFQAYQWNLRAGLSALGCLVLVYVLLELAQI TPRSPHRRLNLASLLGGRFSKVEDPSGSKQYLKKGQLFDFLTENYIS PLLSRAPDAPTSFLFPGAYLTALEAKAISHLKHTRPFVNLTGSRFNE IFDILNQKLTFRDAGSLIQAQTSLRLTAEEGLAAILSHPSPPGLTHE IMKSQFGVYDDYDKVYFLVLGYLPVATSVV JM 33 MTVANQCKHAATLEALPASRKRAGIRAHLAVYRRLIKHRSLDDILKF SEQ ID NO: 34 LSIRPTREATKDVKFRIFFEVTLGRRIADCVLTVDSEHQKTCYVIEL KTCLSAAVFPGNAIKISQRWQGLHQLTDSVAYIGRAAPRGHENWSVR PWLLFKNQKTLKTIHTESSAFPPTFINTTSVALNGFFSQWEDAHVRK MLYEISTKTSAANYRNFLGPTSKQRSVHSQTIADRRKKKRVCDAKST AGAKGSHAAKKPAPSRARQRAADAPTGNRNGHARPRHNSKHGRGSAV PDQGNRRYPNVNKPTTQNRPSDTWRRVCCHDSPRRPGLHGKPGSPSG APAQPVHEPKPMAATIRSVVQ JM 34 MAEGGSGFGDELVRQMRDRKPRWDESSDDTDDVDTESTDLEYDDVFP SEQ ID NO: 35 VVDTHGLTSPGSQNYDVPTSPSGTPWELLHPDALYAQPRCPPKRAAV PGGGARPKVSAFSARLQYVGRQSFGDRETRQLTGAQFSSESEHEYAE IPERTTRPVESGDKRHFTSGRRGGISGPSSSKPSNGAGLTRKTKTSL SVSLKMLLRIKDDDVKVDVPRPVTVPVHLMQPHPMTEYRNAFLIYLE GVMGVGKTTLLNSMTGMVPQENVLSCPEPMKFWTCVYSNCLKEQRSI VKQGTHGKSITSARVYACQSKFALPFRATAAGIGRNLQPWLVGNGST KPANWIVFDRHLLSATVVFPLVHVKYNRLTPDHLFQILSLFSAHDGD VVVLLTLNSSEAHRRIQSRGRKEEKGITQNYLRQVAWAYHAVFCTWV MMQYLTPEQMVQLCVQTVSIEDICNMNSRLTHRFLTLTKLHEQSMIP MVVEMLAAVKEHVTLMEVCLGLFKELRKLQILIVDAGEHLDDTCGLW GNIYGQVMSNEAIKPRAVNWPALESYIQTLTSLESNAAN JM 35 MTYPRLRPERRGNYCTRTLCMRSRGAHLKGRPCRAVVRGPRCPRSRL SEQ ID NO: 36 DFNMLDDRVLGIERRGSLPGPSFLPRASTNMRKYRSVLHARLKAGTR DILPLGVGVEFRDPRRQNLVTVRG JM 36 MSLVPAFNRACSTLRYFRIFVLALGRKLGPGKLPRLSIPKTLSSNIL SEQ ID NO: 37 KSSRERGHLGPRTTARHGRPFRWAPRLRIQSVRVQ JM 37 MFNFKIPFLFCNVSCNVSRIFELAQASCITREVNTSLTFFQLIRYRV SEQ ID NO: 38 LLNSSSTVDISLLTGVVVAGVKRTISSPGTFSSLYSYPLITENVITN KHKPWLIGCIAFQAG JM 38 MQPINHGLCLLVITFSVINGYEYNEENVPGLEIVLFTPATTTPVKSD SEQ ID NO: 39 ISTVELEFNRTRYRINWKNVSEVLTSRVIQDAWASSKILETLQETLQ KRKGILKLNMAYVSNKEINFCKSFSSSEIINITSDFNYSSLPGFLGS FDVINHELTHGVLVSKRELFTNALDIMGLFYAIKLNAETFKITFDES KVIISGIMTADWILVSIANSSSEVNGQCVALLFGDPEKFPPLKGYVS YRDLVVVRNDNYAIAVIAPMSHGTMGLNFLPQWLTDIFFSILNSPLK VINYLKGKLFELESKGACQNPSNEQNILSLFFEVTAIHFLYVRNLNK EEPVNVGCVVKHVAALKSLERLFKLCFPAFELHSLNLWTLSHLAASQ IANLPPNNVMSLTMDEQEVVFSMFKLADNNNVNEIILNEIINISDQM YTMYSDIYQLSNTYRQTVMDIYEVLTTVSLTNVGARAVYPYILFTSM CNNVEISYMINQISKPDDITIFRVFSPCFLSLRFDLDENKLRSDAPQ TSKRTGSELAQGASGFWRLLHAFHATRINEFSVINCTRLAWKQVTAL MPLTNITYVISSVRPDHARVYEVSEVFLNSAMFVSAVYPNCSHFTPP GTALHIPILYNFSAPRIGCPLCDSIVLSYDENQGLQTMMYVSMPQVQ ANLFSPYSPFFDNDNFHIHYLWLMNNGTVVEIRGLYRRHALSAIAFV FAFIGTMSALYFLFKLFSILA JM 39 MFIISFKMISFTLLLSASLNIENTTSCSSIVNDITLFGGKLAICDAA SEQ ID NO: 40 RCDNVHKLSECNSNAGKHNLNNLSKLFKAATCFTTHPTFTGSSLFKF LTYKK JM 40 MGSRQPQIGESPITAFNTVTIMQRANNSIMFLPNLKLKPIQHLFLKH SEQ ID NO: 41 VLLQRLGLENILFHFKMLYANTCKAAAPYQREYFESMLSRVKQRLED MVFCLNSIESHNFQKDFKVTSRAPQQLLTATDKYFLMFPPQNRDLAI QVGAEVIESICDGTPLFEVLANLNPRVTIQKETGNNLLKFYALLTV JM 41 MIVTVLNAVIGLSPICGWREPMAKNMSASKQSDCTSESLVAGGCLRM SEQ ID NO: 42 DRSFLSSDVKGALHKVGGAFGSYSCVVFASSFMVICLLFVRVTGGVL TVTWTENGL JM 42 MIKIPDLKARLVGGAVQLSNGEYVCHVVYSSALAAMVGLPGPAVPLP SEQ ID NO: 43 LLFKKFGTIYSNMMPLYAPKRPELSMLRIMVSPRPYALNSCLCVGTD EGERGVSLFRDPVIRSSDFDDTPITVRLKISDRE JM 43 MMLLQGPVLLPACPATATADTPSPANSDFKTQLAIFCCLATNNEILE SEQ ID NO: 44 NVSLEVLDRANETETTFYACPALRRLVLGEGLYPFIHRQGGIVGKTG NEYAGPGLIIDDAIGCTFSHIETHTFLPTVFTYELSDTVWVQRDERI LRSLYCSPLMVCGVNYQSMFRILCRYLQIWEFEECFAAFTRTLPEHL IGTCYQNYFKLLEPFKTLTLARCPPPCAKLHLNYLKFNILGFTSDWI SHPELHRVQTVIIYNIESNPVLLKNLSKQNKFQDIRVASELIIDYQN IVNQSLGVNLQVKINKKDPGKKPYKVVVVTPKSTYYLTFPPEVPIFR VAMCMSVAEHVCHSCDRLYPNTEFLGPGETPRVLEAMFSRIQYAPKD RDHNFIFDANQNPDRHKQVHHDHQTEPLPDMFDPVKHLSLHNFKISV FNTNMVINTKITCRSLTGTFESIIDIPRLTNNFVMKKFSVKEPSFTV SVFYSDNLCNGAAINVNISGDMLHFMFANGNLRCFLPVKHIFPVSIA NWNSTLDLHGLENQYIVRRGRRDVFWTTNFPSVVSSKDGCNVSWFKA ATATISKIYGRPLLKKLSDELDPILSVPYARIDQVKNTIFTTLETRN KAQIQTLHKRFIECLVECCSFLRLDLGALNRAAJRLGAFDFSKRIISH TKSKHECAILGYKKCNLIPKIYVRSKKIRLDELGRNANFMSFIATTG HAFSNLKPQVIRHTIRRLGLHWRHKAKI JM 44 MYIFPHRNAYVFTHRLHLRTVRHGLGSTRRTNPTVPVLFAINGMWRK SEQ ID NO: 45 LSKHVSNSLSLPSNMGIRGMLCRLHAYTAGTSDRHVLSELL JM 45 MEAALEVRPFPYMATEANLLRQMKESAASGLFKSFQLLLGKDAREGG SEQ ID NO: 46 VQFEGLLGVYTNVIQFVKFLETSLAVACVNTEFKDLKRMTDGKIQFK VSVPTIAYGDGRRPTKQKQYIIMKACNKHHIGAEIELSTDDIELLFI DRETPLDYTEYAGAVKTITASLQFGVDALERGLVDTVLNVKLRSAPP MFILKTLSDPVYTERGLKKAVKSDMVSMFKSYLMDNSFFLDKSDIAV KGKQYVLSVLSDMVGAVCHETVFKGTNTYLSASGEPIAGVMETTENV MRKLLNMLGQVDGGMSGPASYANYVVRGENLVTAVTYGRVMRTFDQF MKRIVDRPNAQPNVDDDRDAVADGQDSLAKTPIAAAVIQIGDKLVAL ESLQRMYNETQFPFPLNRRMHYTYFFPIGLHMPRPQYSTSATIKGVE NPAEQSVETWIVNKNNVLLSFNYQNALKSICHPRMHNPIPCGQALGQ AFPDPGHVHRYGQKSEHPPNMNLYGLVYNYYQGKNVAHVPDIALKAT MTTDELLHPTSHETLRLEVHPMFDFFVHQQPGAQAAYRATHRTMVGN IPQPLAPNEFQNSRGLQFDRAAAVAHVLDQSTMEIIQDTAFDTSYPL LCYVIECLVHGQEDKFLINSPLIALTIETYWNNAGKLAFINSFPMLR FICVHLGNGSISKDVYAHYRKVFGELVVLQQALSKIAGHEVVGRRPA SELINCLQDPNLLPPFAYNDVFTNLLRQSSRHPMVLIGDEGYETEND RDTYINVRGKMEDLVGDMVNIYETRNNADHDGRHVLDVGPFNENEQH MAVLEKLFYYVVLPACANGHVCGMGVDFDNVALALTYNGPVFADVVN PDDEILDHLENGTLREMLEASDIHPTVDMIRTLCTSFLTCPFVTQAS RVVTQRDPAQLLTTHDDGRYVSQTVLVNGFAAFAIADRSRDVAETMF YPVPFTKLYSDPLVAATLHPLVANYVTRLPAQRVPVAFNVPPALMAE YEEWHKSPILAYANTCPITPTSLSTLTSMHMKLSAPGFICHAKHKIH PGFANTAVRTDEVLAENLLFSARASTSMFLGQPSVMRREVRADAVTF EVMHELASLDMALGYSSTITPAHVAAITSDMGVHCQDLFLMFPGDSY QDRTLNDYVKQKAGCQRFGGPGQIREPVAYVAGVPHSDNIPGLSHGQ LATCEIVLTPVTADVTYFQTPNSPRGRASCVISCDAYNNESAERLLF DHSIPDSAYEYRTTVNPWASQQGSLGDVLYNSTSRQVAVPGMYSPCR QFFHKDAILRNNRGLRTLVTEYAARLTGTPATSATDLQYVVVNGTDV FLEQPCQFLQEAFPTLAASHRALLDEYMSNKLTHAPVHMGHYMIEEV APMKRLLKIGNKVAY JM 46 MSCCTRPRTRRFVWRFIRCLIFLFISSQVRKPRIGLPTGLWWVTFRN SEQ ID NO: 47 HWRPTSFKTAEACSLTERRPWLTCWTSQPWKLSKIRRLTRHTHCFVM SLNASSTDRKTNF JM 47 MIRVVSGFVNVNHVTDEVLHFSSDVNVRIPVIFRFVPLVSYEYHRVP SEQ ID NO: 48 RGLPKQVGKNVIVSKGRQKIGVLKTVNQLGRWPASHHLVASNFRERL LQNNELAKNFSVMGVHVLRNTTVAQVNADKSQHREAVNKRQFSGVVP VGFNG JM 48 MTGIRTLTSEEKWRTSSVTWLTFTKPETTRIMTAATSLTSVPLTKTN SEQ ID NO: 49 STWRCWKSSFITWSCQPVPTATSAAWASILTTWPWP JM 49 MALDKSIVVSVTSRLFADEIANLQSKIGCILPLRDAHRLQNIQALGL SEQ ID NO: 50 GNLCSRDSAVDFIQAYHYLDKCTLAVLEEVGPNSLRLTRIDPMDNYQ IKNAYQPAFHWDNYSELVVIPPVFGRKDATVSLESNGFDVVFPAVVP EPLAQTVLQKLLLYNIYYRVAETTPTDVNLAEVTLYTTNITYMGRNY ALDMDPVGSSSANRMLDDLSIYLCVLSALIPRGCVRLLTSLVRHNKH ELVEIFEGVVPPEVQALDLNNVSVADDITRMGALMTYLRSLSSIFNL GRRLHVYAFSSDTNTASCWCAYN JM 50 MSIPKIMTVSRDNEGTVCEVAVDNGRHRAMIYYPKITNSSNERAAQR SEQ ID NO: 51 ADVVKEAFDTETPVDIVKQIVNEGLAISKRNCVRLALYLYFYLQYVC FAILITWQLNPHIDPPGLVFAVNPMGPKHVSKLPHPAIVAVGCGTDA ICKNCSVPDIKTELGVVYNNGSSDSGQSAHYGLALLKAAWLVMGNVC PEPVVRQGAELLGPWNRTAWLDFKSAMAATTFCGSRGVLWSPIHEKN LCRPTWNDVINTSSFFTNESLCPNVPGVSEIVIVLNGDA JM 51 MTAHTNGVLTTTGVSTSQPESFQISPFFRVITKPPIMGLFFCVAMCI SEQ ID NO: 52 IALVWYVMRRVYCKGRVVADSCRDPRRPAYEMLNVRLRPHGTNP JM 52 MLQKDAKLIFISSSNSSDKSTSFLLNLKDAHEKMLNVVSYVCPDHKD SEQ ID NO: 53 DFNLQDTVVACPCYRLHIPAYITIDETVRSTTNLFLDGAFSTELMGD AATSAQSMHKIVSDSSLSQLDLCRVESTSQDIQGAMKPFLHVYIDPA YTNNTDASGTGIGAVIAVNHKVIKCILLGVEHFFLRDLTGTAAYQIA SCAAALIRAIVTLHPQILHVNVAVEGNSSQDAGVAIATVLNEICSVP LSFLHHADKNTLIRSPIYMLGPEKAKAFESFIYALNSGTFSASQTVV SHTIKLSFDPVAYLIDQIKAIRCIPLKDGGHTYCAKQKTMSDDVLVA TVMAHYMATNDKFVFKSLE JM 53 MSFLYHNRCKECQMTRVNSPICQFHNVSSLYQCLDCKRYHVCDGGRD SEQ ID NO: 54 CVIVYTRENLVCDLTGNCVLDNVQDVCSYGPPERRAPDAFIDPLVSH GTRESLKSDILRYFETVGVKSEAYSTVVKNGQLNGIIGRLIDATFNE CLPVMSDGEGGRDLAASIYIHIIISIYSTKTVYDNLLFKCTRNKKYD HIVKTIRAQWMRMVSTGDPSRVMATGCFT JM 54 MLAARSLPPSPSLITGRHSLNVASINLPMMPFSCPFLTTVEYASDFT SEQ ID NO: 55 PTVSKYLNISLLRLSLVPCDTRGSMNASGARRSGGPYEHTSCTLSKT QFPVKSHTRFSRVYTMTQSRPPSHT JM 55 MDAHGLNRRSVAGQCDGLFHVILPRGFILANNITCGGRQRFFAHTRF SEQ ID NO: 56 AASERTSKTLYVWGRVFQMTDPGSGDGPSGPWSGLAISLPLFTTNGK FHPFDVVILRAETPGSGSSWTVKFLYMSLIAAYRNAMRGLKDKVSQS TDAAVDGEVHPLTVLKEALVSPDTATRPVSACNPLQMLTGLLQSRVR DDYVTHHRALERPGNVRGQVSAPTRTEMPNGSPSRVRLGFRPPKQAN YPKTWAQARHVFSSRTYYVCVYDNEELDTKWQRQDPRPLSLDWSDPV AYLLEGDLFLGAKQNAFVDSLEKTCRCQNYTIKQFFPVSINRDNDTV DLIKEHFIEACLVIRNQASERSAWVKAALFRNDSNTYWKDVLGLWEH GPHKLGTAIKRPTSEPCNADIDWSWLLCDADITRSINGQSTVCLVVS PALIAWLVLPGGFVIKGRYDLSSEDLMFVASRYGHPAA JM 56 MATQRRDILKSFLNKECIWLRHPGTSAFVRVYTATTAHSAVFDPPVT SEQ ID NO: 57 SEDAMSHNCLNVMIMLMKPKEFGPCVTVYINGDILDFCATEYVAIRE VPGRADLCLIRFGTLSNAPRSVPIPGPLNPHPRENVPGLTKQEIIYT SQTVPPAQIQDAIKGKAFKQINPFVWFDGGAFWQLFLSVDYMLLCPA LEIVPSLARIVGLLTQCDKSTCKICTLAHVHVNAYRGYTPPDSQGTS PSCPCLISCGARHATDVLVTGHVNLLGLLFDPKVLPKVSRLRLKRNP HPVPIEDAMSGVTAEGTEVLPTSQPWALIRLPDLASRVMLYGCQNLK TICLRSY JM 57 MASCICALGTVWEVYIISCFVSPGTFSRGCGFNGPGIGTLLGALERV SEQ ID NO: 58 PKRIKHRSALPGTSLMATYSVAQKSRISPFMYTVTHGPNSFGFMSII MTFKQLCDIASSLVTGGSKTAECAVVAV JM 58 MPAHGCEVGSTSVPSAVTPDMASSIGTGWGFLFKRSLDTLGSTFGSK SEQ ID NO: 59 SRPKRFTCPVTRTSVACLAPHEIRQGHEGEVPCESGGVYPRYALTCT WASVHILHVLLSHCVRRPTILARDGTISRAGQSSI JM 59 MLLTSYRERLQNNLRAVTDGGCENWFRQPPVIISGNDKTERMANPCL SEQ ID NO: 60 GVIHAVNAYSSVLDDYLQTYRRLQEPMPPPTLGKPRISSHATLPRLT EELTNYLRQTCCRVRMADAKDQHMEYQSAQRTHEAFLECPVYAELRQ FLANLSSFLNGSYVPGVCCLEPFQQQLIMHTFYFIASIKAPEKTHQL FATFKQHFGLFETTDDVLQTFKQKASVFVIPRRHGKTWIVVAIISVL LSSVENVHVGYVAHQKHVANAVFSEVIATLSRWFPAKNLNIKKENGT IVYASPGRRPSSLMCATCFNKNVSRLFLNSGSRIALHDWLNPAGE JM 60 MLSGPNGRRQGPAHGIPIGPTDPRSFPRVSCLCRTAAIFSQPVVIFK SEQ ID NO: 61 WELRARGLLPRALSATVNTIAHVLFYRVYQSTRKDTPVICHV JM 61 MFPSSFLNNENPETGRRFVKGVQLALDLCDNTPGQFKLVETPLNSFL SEQ ID NO: 62 LVSNVLPESRPVRDCPQAEGFDFEHIHLPKLTRMQRVLGRYCDHVNN DDDMCVNVKARSSNAQGALFYLPYGQDEWNWALTLRKDKLVKMAVEG LSDPTTWKGLEPVDPLPLIWLLFYGPRSFCREPECLYERNFGMKGPI LLPPHMYAPRKDVMTFVHHVIKYVKFLYVNAGGGLETELSPPFEASR LRSAIARLGDVEADDAYLSAKCMLCHLYKQNDTISIHETHVGGVIAL GGDGARYITSSVRTQRCTSRGDFVLIPLYNIEGLVSMIREHGLSNS JM 62 MWSFGDSSSTGTDSSLSVPRISSSPYSSSLRSRTASVTASNSSIFFL SEQ ID NO: 63 LNPFSNPNSLCFSRSDVSSVPTTVARLSFFFRLSYDRSDSLVPLYCA LNTALSAPNLSKTEMDSFLLISDSSSDLINNFLAVAEANFPYHAYEP FNVVQRD JM 63 MASATAKKLLIKSELESEINKKLSISVFDRFGADSAVFNAQYKGTRE SEQ ID NO: 64 SLRSYDSLKKKDWLATVVGTLETSLREKQSELGLLKGFNRKKIEEFD AVTDAVRDLKDELYGELEILGTLNDESVPVEEESPKDHIIRWKLERL PRVCPKSP JM 64 MNLFPWKKSPQRTTLLDGNWSVCQECAPKALDPIPKVQTDLDRTALS SEQ ID NO: 65 HITVIRTRKTLAQLKIPNTWSQCSHQATDWTAVLGRGSYGVVRSMSL GRCVKHFGSRREFFYECIFNDIVRARREKHPLNRGGDRILCFLEPCV PCRALIFPQLTGNLLNADFKHVNPERLAVEFSELREGVSFLNNICGI VHCDISPENILIKGELTTAYWRLMIGDLGSASLHTGTPWTGVMVTSK LGFVQHTYHFKAPARFICKHMYRPSCLLYRCLLSCAGGPQARMLDQP FQITPQLGLTIDMSSLGYSLLACLEKYLQPADPFPQQGALADASSES AHPLFYLRCMVPRVVIAEIFSVAWDVPLDLGIDSSGHAPAIPLREAY RRFFANQCSLYRAQYKEDALENASSRLCNSKLKLVLQKLLVRDYFSH CGNCGDHGFFLR JM 65 MDFFSDEPMVQEMALLDIDEQQRHLSKMSLANFLKHERVRAFFNDNK SEQ ID NO: 66 KKISMPAIRFVYNFYLFAKVGDFIGNTEVYDFYVSCVFRGRRLTLLS DVYDACLNMHPHDRHHVCALIEQVTRGQNINPLWDALRDGIISSSKF HWAIKQQNSSKKIFNPWPIVNNHFIAGPLAFGLRCEDVVKKILATLL HPGEAHCENYGFMQSPHNGVFGVSLDFGINVKSNPKDGLEFHPDCKI YEIKCRFKYTFSKMECDPIYAAYAKLYQKPSMQTLKGFLYSISKPAI EFVGEDKLPSEADYLVAYDKEWEVCPRKKRRLTAVHHLVKKCMIHNS TAPSDVYILSDPQETGGQINIKAHLSANLFINVRHPYYYQVLLQSLV VQEYISLSKGTKNLGTQKNFIATGFFRKRQFQDPSNCTIGEFAPLDP HVEIPTLLIVTPVYFPSVAKHQLVKQATEFWAASASEAFPELPWDLS SLCANAPPTP JM 66 MKISRSDSFILSSWVKLLVILGLMFIMSAVVPLTATFPGLGFPCYFN SEQ ID NO: 67 TLVNYSALNLTVRSSAKHLTPTLFLEAPEMFVYISWAFLVDGYLLCY YAWAILAIFKAKRVHATTMTSLQTWIVLIGSHSVVFMSILRLWTIQL FIHVLSYKHILLASFVYCIHFCLSFTHVQAMISCNSATWSLRVLEQQ IPENSLLDTLLRYGKPIGANLYLSLIANEMLVFSLGTMMAIGNSFYM LVSDIVFGSINLFFVLTVAWYINTELFLVKYLKHQIGFYVGVFVSYL ILLLPVVRYDKVFISASLHKVIAVNISMIPITCILAIILRIIRNDWK WCAKAPEYAPLPQGSKEKTTKVKYSPELNALYETEEDVSDDEDAYPK YI JM 67 MYTVYKRGQKYMFVRQHVNKQLNGPQPQNRHKNYAVRTYEHDPGLEA SEQ ID NO: 68 GHCRRVHALGLEYGQDGPRVVTQQISVHQKRPRDVNKHFWCFQKQRR RQVFSRTSDR JM 68 MNAREVALTGHVLHISLHSTHEREKLIIWQVHLLVCQQCGIQGDAAY SEQ ID NO: 69 LFVTETLSNTDWGNIPAINRHAPSMNEHGRNYMQWELRTRLRNPIIQ SLSRQPGAVNVRVSEPNMVIVSCERALHHSCSVRVTGAYLHCNTTMD FRLDSNVSPTREFWFSEMFSKCLVSNIEVYLKTTGGLYYRASSATQC RKRAKDGALGILDIFNCESREIQVAGQKYNLSIATATFHVLWVDEAC MWNGALAEFFRALHNKLFGDREGVAPTLTYVCPGATPEGTPFPPYFS AFPHLLLVFGRPRRLDVTAVQELPKAQIAVHWPPFKNSILGDQLLIP GISPKKPGTVPVRWPLWVQDVNLSLCETTESVARIVDPHSIVIIKIS TLLCQHLKCHRAFVKNELEYIATICSSDLRLFIQEEYNRLLATIFTW AAASGYTWAAIDKTTVFIKAPQLSAAVSGSCPSLNSCRRKQYYKGLK ITVHFLSQEQQKVVTRLEAQLGLPVQETSRPPDWLKYEVCSASVFLK IPAGVLYAGLAKDPVSEAKRDSWLDCLVEGATLSLNNSVPPIGALAG ILPTLFAKRRCVNFWLLPREWVKSAPICPPLPIDCVTPQQFVVTKRG PICWYKEWPLPXTDVDFMYYLQEALCVFSVVSNGEGTESHADDIRQLE KFEKVLCLF JM 69 MNTVVLSMAAQVYPLAAAHVKIVASNRLYSSWMKRRRSLEQMVANYS SEQ ID NO: 70 NSFLTNARWHFRCWHNSVEIFMITIECGSTMRATLSVVSQRLKLTSC TQSGQRTGTVPGFLGEMPGMRS JM 70 MDQILKRLMGEQHRSEAIMPETECASRGPYNYPVLPRLMLEVHKKNS SEQ ID NO: 71 ICMASNTPKLCVRGRLNVPDLGVHVRTRLQSATFTGFVFACVVEHED MVNTLDIYPHVFSDRVQLFKPASASVTELCCILSMLENYDKPPLSFI LSALDRARYLHERYTCNDSAFILYGIEVIASTLAAYHELNPPQGVLR VPPLVRFKLHKLLDENADDMKGLLKPIYLESFRLTENVEEDSHGETF NIFYCGTIFTRHLHNASVLKYFQITSLHSLPRQTLF JM 71 MGFSKPFMSSAFSSNSLWSLNRTRGGTRKTPWGGFNSWYAAKVDAIT SEQ ID NO: 72 SIPYNINAESLHVYLSCRYLARSSADRINDRGGLS JM 72 MFKMNPGLGSTCLVHPTELSISLFEILQGKYAYVRGQTLHSSLRNPG SEQ ID NO: 73 IFGRQLFIHLYKTALGSCTYDNVLKDWTNFETTLKTRWRGVEHLTPE FKRSTFESWARTVRLTVDQLLLNTINQVLHTRTVLSYERYVDWVVAL GLVPIVRRAPDGETIARIQAHCQQMRKTHASGDVTISRIVDKLAQEI TAIMTDVTSIYIPDYAEVSVEFNGDKAAYLGTYRQKDITVEVVSRPI IYNGRVSFDSPLYRLFTAIMTCHRTAEHAKLCQLLNTAPLKALVGST CNDMYKDILARLEQSSQKTDPKRELLNLLIKLAENKTVSGITDVVED FVTDVSQNIVDKNKLFGTGTESTTQGLRKQVSNTVFKCLTNQINEQF DTISNLEKERDDYVKKIQCIETQLLQSLPEGGRPRHDINILTQNTLQ ALSGLRDPTINLSECHIPKGSSVVNSFFSQYVPPFMEMLRELTSLWE GEMFQTYNLTPVVDNQGQRTSIAYSQDTVSILLGPFTYIIAKLTHMD LINHSLISLSLHDIADQLYVDSRLFVYINDIGHKYCEQIIQPGTDGP NTEAFNGGAAPIGGNNA JM 73 MESSVGWTKHVEPSPGFILNMTSDAKVRGVVDHVSRLSNITTSPPEM SEQ ID NO: 74 GWYDLAFDPAEDSGPFLPFTVYLITGTAGAGKSTSISALYQNLNCLI TGATTIAAQNLSRRLKTFCPTIFSAFGFKSRHINIAVRKAHQTGAVS IEQVQQQELSKYWPVIVDIMKEVMAKKPNGMYGTISNADFETLSRMT GPCLWTSNIIVIDEAGTLSSYILTTVVFFYWFLNSWLNTPLYRQGAV PCIVCVGSPTQTNAFQSTYNHGTQKTEISSCENILTFMIGKKVVSEY VNLERNWALFINNKRCTDLQFGHLLKILEYNLPIPDEVMSYVDRFVV PKSKIMDPLEYIGWTRLFLSHSEVKAYLTNLHTCLTLGGDTRDTKLF TCPVVCEVFVKPFEEYKRAVNLTHLTVTEWVTKNLFKLSNYSQFVDQ DMSIVATESTERSTQVTFITKFVKNSHVSLNGKTKKCICGFQGTYFE FKRILDSELFVETHSQDRPEYVYGFLNTLLYNAMYSFHAYGVTRAHE KYLEDLKFAPLPTALATGRVDFQTVREELNLEDDIFYHVCSPPPPAG ITSLQVLVDTYCALKDVFASRIKVACRWFGGEFEKETFSAFTVNMVV RDGVDFVSPSERLNGLLAFASTVESYKIKGYTFLPIAFGRCQGLPLS DDLRKKMPSLVVQDSSGFIACLENNISKLTETMDDGSVFQVCCAGDY GVSSNLAMTIVKAQGMSLERVAVVFGAHKNVQTSHVYVAISRAVNSN YLVMDSNPLKTLLREPVDNTSAKIHIVRALHNPNTTLIY JM 74 MVSVSLDMLFSRHAIKPLESCTTRDGIFFLRSSLSGNPWQRPNAIGK SEQ ID NO: 75 NVYPLILYDSTVDANANNPFRRSEGETKSTPSLTTMLTVNAENVSFS NSPPNQRHATFILEANTSFRAQYVSTKTWREVIPAGGGGLHTW JM 75 MAMFLSDPPRTPPATPRMLPIPGAPRKKRTRRFLFAGSRTGLPVPPG SEQ ID NO: 76 YGGPPVIDMTAPNDVFDADSPPTTPKTPDETDSHSENSNYSDMDEED EQPVSSPPRTDPHARDGESFNQSDWRPTVITAAGPAAQPSAPAPLTA FGGQRPVAVVTGQHRAPPSSTSDSGDDFFIDDYEDTDESGEDADGFS PRASPAWSGDTSRSPAGGGWSSNEEEEPAVTGSAVEQETIIISDDDD TDDRGSVETWDESDADEGTGATDVIDLCSSSDSDDDADHVTSGGVRA ACKRHASRRDCNGDDDVIYLGTTPAPKRRMTSTTGGGATSNPEGPGV SGRQTMAATPPVCGNDISIYPWPWLD JM 76 MRVGFVWRFWSGGRRICIKNIVRCSHVNHRGASVTGRYRQPRTGPGE SEQ ID NO: 77 QKPSCSLFPRCTGNRQHPGSGRRGPWRVRQEHSHDQNVHL JM 77 MDTWLETVVWHKMSMTGPNETPTQMLLISDSWLKFLNLSPFLKKKLA SEQ ID NO: 78 ALLRRVMDMSKATVIYPPIDRIMWWSYCCEPEDIKVVILGQDPYHRG QATGLAFSVAPDYSIPPSLKNIFKEIANTVPGFTAPSHGCLDCWAKR GVLLLNTILTVERGKAGSHSNLGWDWFTSYIISCLSAKLQRCVFMLW GRKAIDKAVLINGQRHLVLKARHPSPLAAAHAATGSPWPQFLGCNHF KLANDYLVQNQRGAVDWNIN JM 78 MYTLSFFTTYFILYIGYSSGLIPNPCCDIVPLTGVNIPAPFEIVSFH SEQ ID NO: 79 FTDLAWCQGRCVATLRYKVGTITTELCVNGFHLPAFFIRILSGLDFS VHREELDLLNYVRISLEDFLSAFKDTHDNSESVTNLPAVPDLTKKGS AAFRTRKVGARRGDLWILGSRQ JM 79 MAVSIPVQGVDRETESNWRSIVTTFEQHGNADRAIRSLLRFFKGVDH SEQ ID NO: 80 PGFLASLVILKDVAIDSEKTIERTDIIPLLQGVRFVTQQIYMHLKDH ASESPVTEIWRDCKERFCLALELACGCQSCTSAARQLRDCQQACRPP KLNPHKQQCGAARLLTAVYNQMVLRTRVSVSEFCLNALMCVPREFGF VSGDVRVETSRVASCMNLSWLYLILDSYIRTDLTNLEMAMSRACRIR GLSTRDPFYSALVWLKNSCACAANTFFFTVNSTRVTTPILMDICASL AGPVPDVIKINMLPLVNNQMYPSVCVERANFTGSCPKMSPTHRFDGL KLETTSLTLAADSLDDILQALELICDDDEGILDSHISDIDTETEVDE STIEEEIVFEELS JM 80 MVDPFKKSQKRPDGSIRVSMLFKGSHDGSPVRLGLPVNTLNWNGNSH SEQ ID NO: 81 DTVNFLMSPKTNPETELNTNDCHPYPKPRPRTIRPG JM 81 MDTDDNQVIKLFFIQDSGGRVYSGVGGSISRRWEWLMNPHLVLGSGA SEQ ID NO: 82 LCILLVQLNLNLACLGRTNQKTAWPRLLGALCKL JM 82 MSRHYGKDHLLNHMYKFHYPPLGMIVGEMNTLTVNARNPLYQAATLR SEQ ID NO: 83 VERALYLSKILQVLMQHRQGERFIVPQCRSNMVYCLKELHKITNDRI RGLINSVLPLVDAGCVGFDEELVRILPEILKLEYPHVHELLPPHDPT SPLSWCLSHMVGVTKTFKGEVKEMIDTFHDLSVPSFQYLASLVKKFF LVEEVIYEDYQDTQFNVFLNLCFFWTTVIKMYQSCIFKDKLLDTIKA CIELLKGEAPQFFGWYDLNTPNLGSAALVKYTEHLIRALSVDSSAIP IGEICSHLHHCKHALLNLE JM 83 MGMADESTLSARIRCSVYFTSAAEPKFGVFRSYQPKNCLASPFRSSM SEQ ID NO: 84 QALMVSNSLSLKMQLWYIFMTVVQKKQRFKNTLNCVSW JM 84 MECASLGPISGLIADLNLFNLFCLYRGSRVKTRGAATCNVPCAECAQ SEQ ID NO: 85 GVVRILTERALCCTEKMFIASACSGVVLPPQLAKVFHDVYAEMKAKC LGAWRRLICCRRPIMAIADSVLVTYNTLDAEGKLDLKLKALCKLVFQ PIFLQRILAPMQLLANGKMVPDNYFTITGTAEKRRPVVTGSTSGMTC PGSSLVPDSLILPVCEPGLLPAPLVDLSNVLENPEIILSAPPLSQFV ITNTHPSLPQSVSIITPTQGVVPGQCFMDTWKAVSQSIHHQAHTPIF AATLAGSTSAAPGPHIACSPVAGTSRQVEASAGVDCGKPVCAPQPDI PPHVPTKRMETVAQSGNAPVKNVHIGGRVYAPLVNIPIIDLTSPSGS GQSPVNIANTPESRMAAGSPPFAETAATVPAKRKQPREDVADKRSKG DGRGAATVNPPFPGPPANRVREQGLFDLIESSTDVTANASGPKNDDD MLAAILQDLYGLQSPPAIDSPSSNSDNEDIFPEVSPPSSGHGSP JM 85 MSSLSELLEGESIAGGDCRPYRSCRIAANMSSSFFGPDAFAVTSVEL SEQ ID NO: 86 SIKSNKPCSRTRIAGGPGNGGFTVAAPRPSPFDLLSATSSRGCFLLA GTVAAVSAKGGEPAAMRDSGVLAILTGLCPEPDGDVKSIIGILTSGA YTRPPMWTFFTGAFPDCATVSILLVGTWGGISGCGAHTGFPQSTPAD ASTCRDVPATGEHAICGPGAADVEPASVAAKIGVCA JM 86 MPRVKTQPKRPQVFDFMPLDLHGETRAEMDSQSLCPDGQDLLGSYIY SEQ ID NO: 87 TENNGPFSQMMHNGQSNNGTGESFGSYAAGDGFLGGSVSGMHGNGTV DGLCSKKQSACRKRSAALIHAASEASVAEQGTSQGTNAVSDRIGRDG GIGNKLLKVSARLPDKTKTLPDPSLNCYF JM 87 MRIYGIKGLNFFGIMGFWNIPLGWGLCFMVWVAWIARGRSVCPTWHL SEQ ID NO: 88 TDGKYEAVYRHYLEECRKHEGSGSPDGSGKTEGSGTKATTEANISIR PNVVTSGQDKEPMKTAPRAESSHDLPRIEQVNALHLSTPELAQPLPV VESTPRESQSGGTPWDARPHAFIMHTNDMLNPSVVLSFRAVRARSIR DTEQSIRDRNTVTTSYRTPGRPSLVQARPSSYGARLPPSPRTMARYA ETRPTDDQN JM 88 MDCSVSRMERARTALKDRTTDGLSMSFVCIMNAWGRASQGVPPDCDS SEQ ID NO: 89 RGVDSTTGRGCANSGVDKWRAIJTCSMRGRSCDDSALGAVFIGSLS JM 89 MSSTRPKTRAPKKELTMEELAAQVQKLSVENKQLKKLINSGDPTRSG SEQ ID NO: 90 SDPVISNSEKEAKIAAAVSALCNVATRKIEAKVPAVTAKAVTRGQVE EALAGINIRVDVSMDETTRGGITASADGALRRRRAQSRTRNNDAD JM 90 MTGSIVLALALTACLYLCLPVCATVTTSSTTGTGTPPVTTTPSAAPS SEQ ID NO: 91 VTPSFYDYDCSADTYQPVLSSFSSIWAVINSVLVAVATFLYLTYMCF FKFVETVAHE JM 91 MAEVTAHTVAYAFDSCKFEIIPKNNSSRIALRNKFPVVVKPGEPLVV SEQ ID NO: 92 PLGLRIIRAPQCAFFLSGAPTDEVYYHTGLIDQGYRGEIKIIVLNKT KQSVTLYRGEVNVSLIAFMYASPGPLKCPILNLPHYSLDAGFDVTSP HAMTIPPTDRTPFTLSLYYKSPQLSTPHVPLIVGRSGLAAKGLTVDA TKWTQSLVHLRFYNFTKEPIDIPANSRICQVVFIHEDHVPSGWNILR SRVQLGSTLQISWAKIRFTDVATLPATHPLNSRPTQSQTEPETNRGA KGLGSSGL JM 92 MSGSVYSRRPRPKRVEHSEIPRTTRQHPPDIVGQNQVHRRGHASRNP SEQ ID NO: 93 PAQLPPHSKPDRTRDQPRRKGVGVVRVIILKHGIILKLFIFWKTIQI NINHQPGHLVLFCLARYYPPPPTGASVVESPDGRGWRTLRYLPAHY JM 93 MAAPGSFWTCCGFSPFGRVGCRYRPLPDPLNECPTHWRTEIANGLPP SEQ ID NO: 94 GVDMGDVKQAEMCTAALRQTYLLAVQSNKITEYLRRFDAARVPAGCQ ETVRIQISKLKSIQNVIWNAMLSLAIGDITVDESAFHALLNKRADET VSLLEMEKLATTIASDDSVTWAAEINNVLVDTEASSNPSHPVIRQPT PQLAVADNIVPDKIIQDAQADG JM 94 MSQVRPLPDERVNEIRAIFSTSGDMAEVITDILTGTQATASFFCVLH SEQ ID NO: 95 DRGNVPINTPHAVIKLCLPARRPGGGPRCLPLMVLNLPAWQVHLFLT GDAPLTSDNIKDRIDLAQTEEILEPILSVLACKRSAQQTKHDSFKSK VAWFRAKFVSALRKVYKMTPSPYWMITLLGSFEASFVLAGTFYFFQS YTCTAETLVHLTRLFISSQGQSLVTVNTYDELGRVFGRSDFLEIVPN FWAYLKYKMQQDDVESKAIDQTINSIRGGLMLSPQDLVHFIYLSFYE CMNAQTFLSYSRTTASLPTPATVNPPQLCRRLEADFKEHVMAYYNKA SYLSTYITILTVPAPLPEGYENFQELACQYWCGQSRDVAEIMTRIND QYPQLNLTKDLSGLLDLAALDQDSGGPKENLFTVASRIPTYRCEFLN KQYFVLMHTDCIDAYWKQNIIVPEDAQLQGLTDQDLTSRIFYCDLGL SLPTFKQQIMVSRHEYFNPRLPVYRWVLDFDLKVTEGRRTLNDIYNI CVTLRQVILETLQLIGPLKPHHPVYFFKSACPAVTWPDDISDTAFCH CDTKIGMRIVTPFPIGYCLVGSAPLVSLTNILNRVVKLDTRLASEYP GILEDKGPFDSGIYAKGRCVRVPHCYKVGPGGELSRLLKIIICHPEE SDKSAYLKNAFKVSNLLHHAPGDSVTKNGHLVYAIADENEGFLESKT KNNLPKTITDLAEKIERTTEKPLIDWAATAVWPKLHDTIQRFFPDDR IGQFASVSFMHSGDNIIQVRPQKGNNFFCINHKHRNHTQTVRVFLTL HSTKESEVTVTFMSQCFAAKCNHNSPTAHFSFMVPITCT JM 95 MLSPECMKLTDANWPMRSSGKKRCMVSCSFGHTAVAAQSISGFSVVR SEQ ID NO: 96 SIFSAKSVIVFGRLFLVLLSRKPSFSSAIAYTRWPFLVTESPGA JM 96 MAQAMVSLEYMKDILDGKKTSYGSYNFYLKPQLTKRLVLYALHAVRV SEQ ID NO: 97 SRTNLFYRGHIIIGLRRLLIGRDGRPVPDAGARTVHGTAQLS JM 97 MRYVFHALICFIGGISSSDFDDSSSDEMDDLSPTPEPEPSTAPHSFP SEQ ID NO: 98 EGPKSKVVALPKIRKRSRSKTPVKIEHRSPLNRSRSRSRTRSGSGQR TSSTYVKRFKPTVDAPRSREPWHRGGKGKAPFIRRNALAERGRRTYG NEHRGKSALTRNIKESIKKMHLPSTMLSRPHDKKVFEGLLPRHLEQC FQVCLPAPPPLRPEVFTDRQLTAIVKSGGRRDALVAKKVSLAKVMSM YKPLLTFVTGRNNQAHWLATRKNTLASAGLEALAAFIEEGLAWAQVC VSQNRSLNDSNLDIILDSSQSVCTWFISKIRHLHIQCFLENQGEISL VKQLTYLVCINNRLAEAANLAGEVKLNFKFAMLIGFALTLPALLAEQ KLSGESLYLFRSFLEKYRPGDVMGLLNSIVVEHYTKCRSAECVITTR AMVGSGENNKGLFFFPA JM 98 MATWCPPNSGGPSAMGLREWIVTHANLGTYSGLFWADDEKTRVVLAT SEQ ID NO: 99 TTAWTVEFDYPRDGKVYEDYCNQRNIPLPSGRPRLCQAKARLLGAIR KSAYFVEEKNFLRRSFSFPTVVFRLRSNEEMSCRLCPRASGVAAELR GLRFRMFKRKGADDVGRVTEYTVKQLLGLLRTRHAGASTMTAPATEA SATTAGEDGRQDESEGGAVALPEEHTPPLSVSSGLSACLAPSVDDPW GFMHIQVYYYGFLQSQVFTRTGMGVRLSTRPTDKNEHHVCMAHGPLQ LWLPPAPHMDDDVMLSRLVNALNALEDGIVLSSCQYGIMMNGYGFLN LWFRGNTLNTLEPTRVPSGVGHRIFDTDDYITKLAQSPRPSDPGPPD PFAQIWVAAWSLYEEEDLSQAPICIIVHQREIYRHFE JM 99 MAPNTQKDRLIQIAAECVPRVTQPRPLHSRPAYRLHRRWLRTPRWPG SEQ ID NO: RSWWRHRRDGYEAARAAALPCIQLPCPHRRRPCA 100 JM 100 MRLPVGADVCSRHEIIPPAATNSLSAQSAGYRLISLTSTPPHHLHRS SEQ ID NO: CPCPDCPLNLVRSRPALLPGQAIDSSPLRDLPYGRNRRHEPLMFQLS 101 RGKNNPRCRTQTRFRTRNAVLWRWVHGRDSATEPTDTGRFVHIJL JM 101 MAGRGVDIKAWLVAAVESSEYHGLVWENEDKTVVRVPWNKVTAARSD SEQ ID NO: SEKFFDDYCNMRGICQGEKPPHYGRFRKMRFLYDMRHHKSIRELKFI 102 NKAYGRSEAPYRLFRLLPEPVVSCANCNLMSSTETQCLGLTSEFRYD QWGGFGRERRRVFTATVLARSWMDKNKRVREHRLPGAIQLTFLYFGS TVGLERVHAGTRVCSRPYPVLAGHACCFQDERTLFLPPPGVVDCSFA REDLRGMHKKCEKGLLIALTDTGISVKNLENREMKVLTNNEEEYKDL PSRQPVQVFDMVDYLRALARSPKPGDDPPRDYAQIALCLSVQSPNPA HAPIAIRLRYVCETSSVCGTEGCFYPGTIGTSEARVAGSFHMEDPGE GTSQSLDPAVELGDSGPDSMDISIPDTGTSGEDDGVACS JM 102 MGGIRRLNRQTQGDLCIISRWVVSRLRGPCKSSKIIHHIKHLNGLPG SEQ ID NO: RQVLILLLIVSKHFHFPVLQVLYGNASTRKGNQQTLLALFVHAP 103 JM 103 MERPVRVTKPSSLRGWLVECCETGRHPGMRWIDDERTLIRIPWNHDR SEQ ID NO: GSRGVEESEKNIFIDYCRSRGILHAAGRELTAKECKNWLSSAIRHSQ 104 TVSDVSTNDDLSTPYPNRCRTIRLLPITVRSCARCDQASGTTAMLRG LREEAVNKFGPVGAGVQYTGAVGAGGEQCWMLRITFYYYGDRFGEVV TESPNGTRVLPLSERRAQGHICVAPIAEQALVPEIPSHLVEFQAEAL RFLDKDLLRGLAFWADPSGIYIRWLGHSMAFVQGNVESPGAIVVLSC ANACRAFNLVDYMKGMARTPRDGTAPPQACVYLYFGGVPTPEGGVQS TVPLIIQLWHECLWQALSAANV JM 104 MAIRDSNYSHLRSWTLYHLNEKTYSDLTWCDQEKKTFKLSWKKGAAG SEQ ID NO: TPAVVAYCAQRGLQVGIDGNVFECKRRFLRGLRENAGFQECEHGVVR 105 THGGGWTAFRVKPLMDSGCFACILDEMSEGIINYLEQVCGIGLEPGM PLPAPLPTLVPPTRSAYARAHRLGVPEAPLPHQIVPFWRLRIQVFYF GVLALDHTSQDRRGVRLHPRPVPRPGHLCFYGTGFTVWFPSPDPGKL TPDQITQINTMLVTYNEGIYVHGNETGVYVDNRNRETLYAAGNDCNG DIIQREVMFLSKQQIFYFMGFMRKLARSPVPESHAPCNGATLYLSQQ PGAQESPQVPISVVVCQDELVQGQMNPSRWCA JM 105 MALWYRGAGKLSHETHEIKNLLFREEHDLSLNNITITVVTRSVKRFP SEQ ID NO: VPIIDVHSGFIAVYVDALVIRDQHCVYLRYLIWSQFSRIWRWKPNGK 106 PGAVKTQMTGTWNRARMQTNTSSILGRMIQCQNAKIKHLNS JM 106 MAAGESRRGPSRYGMALREWLISKADSGFYPGLFWADEHKTRLVLAA SEQ ID NO: TSPSLPNYDYQRDGQHYDAYCDLRHIPLPSGRGRLCQAKGRLLGAIR 107 KSKYFDEDKDFPTDQFPFTAVVFRLRSFEEMSCPVCPRVDALRLELR NMRFAMLGRGMLHAFPESSVGDHEARHLEGQEGGDDARDDDAPYSSG VLRARLMACAAPSAGDPWGHMHIKIYYYGQLQAELSTATGQGIRLSS RPTNKSGHHVCVLDGPLQAWFPPIPQITDTSMGQRLEDALKWLVDGI IFCSTSRGIVFTITGAPNVWFQGNTVEPRNFPHRAYTGMHVWAFDTD RYLLDIARSPSPHDTDPPAAFVKLWVSGCSLGEERNVSRAPLSMTVH QTEIYRHFE JM 107 MTQLRPYCDKHRESGTRVLLWPFCQMNPTGNIYFLQYGAKVETEVLP SEQ ID NO: VVPEAPPRTPDGPSSPLLLPVALSPVSTDTSSHT 108 JM 108 MAEQNMDLKAWFIDAVESRRYPGVVWDDDDRTIIRIPWNRSTDSRID SEQ ID NO: EEYNKIFDDFCLARGVCQSGSTAHANKFKKIRMLYAVRSHRYLRELT 109 PPSKAGGVSGERYRLFQLLPEVTNGCDLCNLIATTSLHSCSMGSGVR DDFFEQAPRPRARLPLRVSIQRRKARLQGSPAQAAPGAIEVSFFYFG ENVGVEILRSGCGVRICGLPDPKRPGHLCCADNPLTRFLPSAQLVPC EFARADLQALQKTCERGLICVMVESGICVKNLEERNMTALTNYSENY YELQPTQQFQVFDLLHYLRALARSPTPGDLPPRDCAWIFLCPSTQSE NTWDAPIALKLRYVCDDVSVETGDSATGSNSGDEGPSGVRGGASGTT GSTSVSTFAPYWRK JM 109 MLRSSRFFTQIPDSTITQIRPLSHVFCRACKSALANSHGTNCADGRK SEQ ID NO: RVNGLSAQHRCPGRLGSGRPHIRTPQPERKISTPTFSPK 110 JM 110 MRLSVDLFHGIRIMVLSSSSHTTPGYRRDSTASMNQAFKSMFCSAIS SEQ ID NO: RVHHLYRAGQLKYRAHRTTSLRDQKNLDLKEAYLYTPTGQLSNK 111 JM 111 MAEGRAGSIRVNRPSGLRAWLLDCCDNGKMPGMHWLNEEKTLVRLPW SEQ ID NO: NHLKGAGGVSENEKNIFLDYCQFKGIRHTGNRPLSLRECKNWLASAI 112 RHSQTVEDVSTEENLSAPAPYRCRVIRLLPIFVRSCPLCNEADATGG MLLDLRNEVTARFLYLGAGREYEGAVGSDGVRCWMIRLVIYYYGRLV GNMEVGSPNGVRLLPAPKQPLQGHVCAGIKPEQVMLPHNPHNLLPYQ TSMLRWLAKEIIRGLMIYADGSGIYVRYMGHVPAFLLGNGGSPEPVD MINSGRVARVFSLVQYLSAVSATPPHGTLFPAAYASLHIGGVPTPEG EPCPTIPLSIQMWHECLWRACGDAAM JM 112 MAESEITHNHLRRWIISNLEANTYPDHLRWCDEEKRSFKLSWHRGMQ SEQ ID NO: GMQPVVAYCLDRDLQCGRQHNVSDCRKRLLRVLRENAGFEQDDTPAT 113 TTNSGGERFFYLKPAVDPLCYACILDSHSETVINYLEAACVHGLEPW TPLPPQAPAEASGAARSVYARAARLAIAAPPHPEQITPFWRLRIQVF YFGSLVAEHTGVDRRGVRLHKRQDPKAGHACYYGTAFKMWLPTPHEN GPLTPEQRETVCEIINYCEEGIFLHGNELGIYVDNRTRHTLSCAGND AEGNHAQRFVRSCAKFQIFYVMGLLRKLALSPVPGDPVPINAVTLYL GGRPGSRKRPQVPVILVICQDELTHGDIRPARWIL JM 113 MANSWGYMWITEQGTLFPAPGTTQRETTHSVLCDPVPNFRFFMLWVY SEQ ID NO: CANSPFPPFPATRFPSTQSLFTLGVALAPVKDPRSLSFW 114 JM 114 MDLSLGRPYRLKLRRRLVVRRGPFMPEPPGWQLPRHHTRSRSLHFGG SEQ ID NO: YVYKFFILDRWWRNTRAWIVEGYACISAKTQKLANRVIMGQRLRCGF 115 QRRMRMDH JM 115 MGTYTSEASLAWLSFMSGTVAASPFILCFIYHSLYFLEPLNSVENII SEQ ID NO: FSWGAVGLHGLLLLVCVVGPPAWLSRQVDVPCTISAILITAGSMAST 116 LGVDLPWVYVSFFVGSCLCLLLCVVVANDVVYLCPTIAHRYYELGFF AAFSVYYFLVLKNLFLAPVFLLPLVAFIVGGVCSLRALRSHPLYEAG LQRRHAIFSLTSRRYITYSIKQALEVCGWDFYLVTVLIGGAAAGTLS VGLTTPLLLGLVHYFFVFHVGLFCCIGLVFRSNVLALVYVLAAAVLL TLTHVLGPGTHNLFTRVCVFTVFLLTMFGAIGCELQIIRKKLQRAAN SPRIVLGVCACGNLLMAVVFFSLNKVELVAL JM 116 MPVSFHYGARVDVDALGNISKVYDHIKGIVKKGVIQISGQGRAPVLS SEQ ID NO: VLSSVGDAGVLGLRLKNALAPLMVYSDMTDEVSFSFRNTSLGNTFTH 117 TREMFGVNITEMNVAFYHHGDESNAEGKPQFVRTTIAYGDNBTSTVH KSVVDEPNLPSFHDRLEQAGTGNRLFLTVKTLTLLSKWLRQQKTRAK QVVTVSLSETLAVATFTVDGVSKIIDFKPDTPDAKWTCAKGRKLDVG VVSSDLTTHVSLESLVAALNACKIPGFFLPGFRWHANEILEVEGLPL TDSLADVKLGVMLLKVDPTDRNNAVPGNLSEGADPEGVPELPSPPRT PDLDLKEQCVPNAEDGTEPTDGGAKSLRTSGSRPEKKHGKRKHSSSP SRGKAKTKTPRATFNPLF JM 117 MLTPNISRVWVNVFPREVFRKLKLTSSVMSEYTISGASAFLSRRPRT SEQ ID NO: PASPTLESTLRTGALPWPLICITPFLTMPLMWS 118 JM 118 MSGLSIVTAANESPDRFLYASDHPGFLALTQETWQNRWFPSQISLHE SEQ ID NO: DSDEVRLLSPTDREFYQFLFTFLGMAESLVNFNIEDLVKEFSNHDVT 119 HYYAEQVANENIHGKVYANILNLFFGGNRGDLMTYAKKIVEDATLAK KIDWLHSRVRKATTRAEKVLLFLVIEGIYFISSFYSIGLFRLRGVMR GVCLANDYISRDELLHTRAAGLLYNTMISRDESPSVAYIHGLFREAV EIETLFIRSKSRGVTMVNVGDIEQFLQATADRILKSINVPPLFGARP PNACPLSYTSAKSVNFFERDNSEYVTSVHNDL JM 119 MNTETSFSAAKSAKPLTLVTNAETGGCSSSLDPERCAESLVNSLKAT SEQ ID NO: LGWDVEANSLTGLLWHRIMEDRCLVTVKDYLTVFGEKLSDEVREFNL 120 KHEAALDGLLQDFKQSKAYANLVNCGYLSAVRFYDTYVLRTHGSSPI FESVAQMFMRVAVFVACQCIKFPCLRKTLRHLVQSETELDEMYLVGY AFHYISSQIVCCATPVLRSAGLRGGQLSSCFILKPSMATENKTLKAL HEEMSPLLASKSGVGIDVSSFAEHKNITSCLKLINAHVGYFNDNNIR PVGASAYMELWHHQICDFLNAKMPENQERCHNLFQGVCVPELFFRLY ETNPDGQWHLFAPEVAPNLLKLYGAEFEIEYNRLVAAGKHSSSLPLK SMMYALINTVIKTGSPYVLLKEALNKHHWCETQGSAINCSNLCAEIV QQPEGQASVCNLANISLPKCLRPPRGKSGVEPGKGDVTFGFELLDDA VEAAVIIVNACILGGTAPTESVRRGQKERSMGIGVQGLADVFAELGF GYLDAESAKLDVEIFQAMYFAAVHTSHEIVLLGEGTPFHGWERSRLA QGVFHWQTWDGVKPSHPPLERWEQLGRSIAQHGIFNSQFLALMPTAG TSQLTGYTEAFYPFFANIASKVTSKEEILKPNVTFFKRVKPGDLRTV RRYGGDVASFPEPLKDRYKIFLTAFDYCPIKQLERAGAPAPFVDQSQ SLNFFLKEEQATRASYIRDLLLTGYRLGLKTMLYYCRIQKQTKLWAL QCLDQVVGDNTSSEGAESNRVQKADGEQAEVCLACQ JM 120 MTPWRPQLLLSMRAFWAGRRLPRALGAARRNDQWALASKDWPTCLPN SEQ ID NO: SALATLTPRAPSWTWRFFRQCILRRCTRVTRLFYLARGLRFMDGSGV 121 DWLRVCFTGKRGTALSRPTRPWKDGSSWGAASPSMEFSTASFWR JM 121 MERVTNQVHLVQLRFTLHQVSEGLPQTRKFYALTGHKNSHPHKHLGN SEQ ID NO: ALKNGRRAMGSQHVRIVKPDGRQVAAVNEICVCLALLKVLQKTVKGR 122 FVF JM 122 MKTRDANVNKLNDSLMRLLPPPPHRVSLSRGRDFSKGVRDLLSKYVV SEQ ID NO: STTTGVEAIKDGFLSVSPKCQTYGDFLIYSQTMSSQEPRGTYLFSFK 123 QTDTGSSIDMLFTPTSLARLSRMDADSAPQTNRIACVWYGHESGLLD AIPNFEELLETGSLHQFLAPVGPLVQTVHSTFVTKVTSALKGDVVAP EPVVTHIGLTLPSDMFVDLDDSCPSSLRDEPLPAHSSIYVCLTYIRA NNRPALGLGFFKSGKGYCEIAAQLRDFYSGVIRTKYIQLQNDLYINR LAFGVVCRLGSVPSGSQPSFQSLHFKGAALPVLKFTEFVSNPGSWKL FL JM 123 MTSSISAARADNGDENTGGLYRLIDNLLTCTGSLQQLKLLMEFQLKP SEQ ID NO: LPTAHLLSMPTVTRFLMTAFKIDNPLVSFIQKHPVFFLMRVARLPDP 124 VITDHQSAETSTGILSEVVNVLNIAIQKPHESPAAKDDDYLDNRAIL TMITEYIHHVTSRTPSGIPPTPPMGISHLPCVEQILHETHRQYWNLA LPESLFIDTGEVASPLQTWLIISYCKKLQLAPPPLFPPADELARRLV TGHHELFVPLSTSLETYITMPVSKRRAFEIYSVFAKSKNIVDGTPIL AFTDTELTTFTPELLFLYDFVIESLCKNQAYGCSRNAIEHFIKKGID FMAELGAFIEKTCGYRSTVSLSNVRSVKARLASCGLSKEACEDFRTM ILMTPHETTPKWENFTDFLEMVNQLTLYGFYFYECLNQYSPTSISLA KIQNILNRVDAEQSDRALWRTPLIGSFPFPWKLNNVLAFFKPSAPVA TLQKIYKAIPSYLMRSLFEIAANKSWGNIALAERAPLTDIQTAEPDQ GPVPTQVIAKYCSRLQISATDYDAVIVSSPGFATEFIRTKLYPILSE VLRNTSKKNRSLFQLRWLIVFAAEDAKDLAPIRRSLALAYFQIMDIL EEKHSPESFYNLLDYLQDTFRCIRQVIPEATCPQEFLQYLFTFQNLP IAASFIQTSMTFVDDLNNGIPGILDLVSLGAAFYNMKLLYDSTLDTV EIPTEEGQPIVVSMFVFKSTIRILEKLLQEAVIALAQTSEPMYAAHI RLMQHLTYMQKIAGHEIMTTQLPSVFHEIHEGYLQCFKRFKRLMLHV TGSCCYSLTRYFGFLYQPPLIPDTIVQKILNFNDKTDTTDDILKSLS QPVGQEPLSAENESSSRLSKNDVELLQKLYDDFRNGSTNDNPTSIKL EYSGNYNETQVSVDWSTYNLVTYTAPDDTLKFTPVNTEALDRMLAE JM 124 MELPPIFSKFKIEGVATTHQADCRFGQYAGSQCLSNCVIYLAQSYFN SEQ ID NO: RESPVTDTNDLDDVLRQGATLDFILRRSGTLGYNQYAQLHHIPSFIK 125 TNEWSAAIFQSQEYFGLIGLDAAIREPFIESLKSILTRNYAGTVQYF LFICGDKAGAVIIKNKTFYLFDPHCVPHVPNSPAHVISSADPTAILE YVSPPDREYTGSFLYIMPSEYVNPEHYITNHYRTITFAKVHGPQIDI STGIEFCTIEDIPSPPRSPDVTSKSSNLARVPKTTTDTSSAKTTPAP LSGLLGVEPPTSYPDPAADDADTKLLTPAPARTAVDHPEFQTTPGAT LLLSELSASRGRKRKLSSLQRYSDSDEASSDDEGAPRRPAHDDAISA EVIWMDDDISPLYSPSATPSFDDVFDSPPMSPEFTYTNATEDTDGAF LEQIVRDAETPFSAFNDLISDHDFSSLDKKIEQLIKYEAPSQHLPNI SDKRNGRAVREAAALQAMDKIMINIILEHGLITDAQARGPSACKNVL QFFILWGEKLNIPISDAKQVLELDLQLIPLHTALSEGKFKQGAFKKH LTTKINRCLASMRATHANAHKKLASAFNIEGSQISSSETKISVRALK EQIANHLSPGFLAVYSADELKHLRDKIRDLKTGIEQRNREIQQEELF FGAVLTALDTFQPPPKPAYPMEIFPHRKTDVMLNHLASITTRLTDDA TEALNNYLETPPDQGTHITNIPNFSSIVANIISTIKILTYAENDMQL NVTPMATYRRQLLYLGGELATIFNLEWPYETVPPVQELPLVARAKAK MESVTKMEKNQQALDQILGDAETLLDTITATSGNENPVRAMSIPILE TYITNAGALIGTSRNPRFEKLKAAIHDLASSESFIIMLLNNTRLDNI SDNLAKIDGILTNNTRFLSTATVTKTLQTLGSSLIRECVEALDKRSP SSLTDARLLAVQTILGHASVPDHETLTRIVSGVASAQKESAGDDPDR WTRVTGHLNELKLAATQSNVDKATRRKLLMIITRDLKEAEVSQETVL ETRWQENVLKFQPSTSKEIEDFLQSAPSAKARKFAEKHLRTLIAQFD GHEQRPSEATAVPMDYTPTPIPTPQAVSTATAEKGKAAWNKIQQAFQ DFNFHLIDASDWQEMASEYSRHGSSLPGTVGPKLVRFMESISNTLDD ILTQKLASLLPNGPAFRPPAFDWIAPYQTRVNAFLKTIGLPMVRDLA DKIHHQCQTVSHAVQSADLQQATVGTSLERPAAEYCRILSDMQVAFN DHGIAVRSEAAAYTDAINSPANVATPPKPNLEAPKKLMTATDVLTVE DFPEFLKTSILQQEQRLIALQRAEFQQLEASISAAERLRQSTRNEIA GKMATAITQLLPRAPVAISSRPLNLSKPIDFLSSTVYDKILDKEPYE TAIAGFAWLETATKSVMVYSHQNQTQQLNVLLSEVEKQSTIAQRLHD LEVSARNTDDVKVLKQALDELAPLRVKGGKTTVDAWKQKLESIESLL RATRTAGEISSELERIGAQAVGTIAVRDLGTLSDQCREAANFLKQAS LPEGFSDIGTKLSELQAYIKYKKQFLEHFETTQPNVFRRFPLSQNIT ENVPARLAMDSMARLANHLHVRGSAPHFTTWIETLPTVDPEKPTHVP AHGGAPLHRQITYSNVLEALFSLCSTTLTPVPTAPGLEIATRARRGA EAATWMDRQWPDIAQTLQDVLDTYEHTTTHANRDATSNAFLAMCVFT QIIRGASRAVTLPKLPGTAVDFPEEIVLTPRECTTLVTAMWPTLAAA ILRLKSYSEALGLMSRFLPLMFQALPHLTLEAQVQNGPHNTPPQVRC FARTEAIPYFPAQWQSANLEQSLWGQTDFLQICDNNQRKARVAAVTW ALTTINGVVLDQLWSTFKPMTAASDDTYVDLVKTLHLTTFGPRGPTP RRETTTEHPPYEYGQPTGYCISGQSTTPVQASNTPGVRF JM 125 MESPTVNIEEIYRRPSRSPRRISHRRVRAYVGPLRRQTTLRRNPNIA SEQ ID NO: EGWTACVSDPWMPTVLKEVAWLPVLFGIRGGRRRFALERELRVLCPR 126 RRLPGLGSLSVVRRPVDRIAVPVWFWR JM 126 MILIIILSIAWRAAASRTARPFRLSEMFGRCCEGASYLINCSIFLSR SEQ ID NO: EEKSWSDIRSLNAENGVSASRTICSRNAPSVSSVAFVYVNSGLIGGL 127 SNTSSNDGVADGEYRGDISSSIQITSADIASSCARLRGAPSSSDDAS SESEYR JM 127 VWTARRRASVREDGLLLSSASTHSRIRLLPSVWSVFVTVAVERKRV SEQ ID NO: LLVRMPSILARLSDMLSSRVLFSSIMNDSDDARSWMAALSFSNRGF 128 REVPIRAPAFVI JM 128 MSRCSCWRIDVFRNSGKSSTVRTSVAVISFLGASRLGFGGVATLAGE SEQ ID NO: LIASVYAAASDLTAIPWSLKATCMSESIRQYSAAGRSKLVPTVAC 129 JM 129 MVPTACAPMRSSSEDISPAVLVARSRDSMLSSFCFHASTVVFPPFTL SEQ ID NO: RGASSSSACFSTFTSSVFLADTSRSCRRWAMVLCFSTSLSSTFNCCV 130 WFW JM 130 MGTGLRGALYRLLNGSTSGTHSRMGVRSPMPPRAWPRRWACRQKDSH SEQ ID NO: WYVKHHRSEHRLKSGHPACLKPGPAWSIGPRCSSPWAVRTRTAGARW 131 SFLALVLDRADQRWSGVGS JM 131 MGLLTPILECVPDVEPFKSLYNAPRKPVPINTLPASLHPHDEQQVFL SEQ ID NO: RQAQWLSYRFIPHEAARSSSPPLLVVIDPENLVTATYSSGGPANFES 132 RPFYVMPGPYPTDWPKTLSVTSNTSVTHLSHDEICNLFTTLSREHGT VQGRDIFAAAPTNVTPERTANHPTWETENQLTTQTEPAEKTHVIPAS PKARTDPIAETTAHHSQGQASQHANNVNQPGQITSHASRNKPSTAPQ ASSRPEKLNTQTVPRLISQTSETAHINHPASGQVTEPKGIFGTYKPR VLTEPAKPAHASIASRQPEATTTVPKLPINAPTAKVFIGTASKFLPD VEESHGTTPGAHQSKIDQKQYGESQPHRTPHLEEVPRAPHVDTPTSA HINVPSSQGPKTIHARVTPGIQTVTPSAPPPAGQIRAFNTRFPEPTA GRSTTNRMWN JM 132 MLYFQEFGGVLVDESLRLDRMGRSIYSRPVRACETHFVFWAILLPHW SEQ ID NO: LGSIPHPIRRGATGRRFWEACIECADLTGRWGGAGSYCLNTGCYARV 133 YCFWTLARGDVYVCAGWSVDVRRPWNLFKVWGAVRLTFAVLFLIYL JM 133 MSSLRVKEPIVQGRLEHDYPNHPLVAEMNNLPQGDMSPAQYAIAKRN SEQ ID NO: YLVFLTAKHHYDMYTQKKNGILRKDHLRGLRGKKDASSSESSVLSGS 134 GSAAPSVAPVASTLGSNSFTTISSGPHSLIGSIGPTPGGGGPGSVAS SGIGSTSLSPSDATTLDTRRSSQNKKSK JM 134 MPEDATLPGPPPPGVGPIEPINEWGPLEIVVKLFDPRVEATGATLGA SEQ ID NO: AEPDPDKTLEILELASFLPRRPRRWSLRKIPFFFCVYMS 135 JM 135 MASGRLPDLAEDEAACHGRVPYPVHHWLDCSRLGLDFAASMRAIGLC SEQ ID NO: PECYVCFVTYGLGAWEGQPPEWARTLISAPSFQTALNDIATGWMPDN 136 PPKNGDVKSRLHDTGRLLLEAYAWVLRCICTGVGYADNEGLSLTAVP RGAWSRYLVVSFPRACCFVCKTLNCRQRFPLVTCSPQHALDLPVLRK KWNGAGCVAMQLNVPSESRRLGANLDERGLGPSDAGLLASLRELAPT VPCGNPFNALLRSLTFRGLLSMSRVVLPIGESTETEISRDLGQKVLA YNVLFPCISLPVWSQVVARSVLEKTVPAPRVVVCLECGYCLNFGRGK FETVNFPPTNVFFSRDQKEKQLSICATTGRVYCSYCGGSHMRVISLF EITCVGDPYLRCVLANNAAHSIRDANSLVSVVVPCLASPDCATGLLK HLRVAELFYLTSSISSLSCGKCNRS JM 136 MGSTTRDMLNRPLNVRLLRRALNGLPHGTVGASSRSEASSPASEGPR SEQ ID NO: PRSSRLAPKRLEMDGTFSCIATQPAPFHFFRKTGKSSACCGEHVTRG 137 NRWRQLRVLHTKQHALGNDTTRYLDHAPLGTAVKLRPSLSA JM 137 MSSGKRLVDELCDVVVSYLGPSGISLDLERCQDGAPVYAKGGAVPVC SEQ ID NO: TVRLQHGCVYHLEFVYKFWLHKLERLAYPFAPCFVITNNGLATTLKC 138 FLCKPRDADAQFGKNLPINSDVYLERNSSVFLGQDDFMKFKARLVFS GDLNVYSSMVICRTYFTEHRQVLQFLVVTPKSAKRLKTLLRTVFALT GHSDGLGALRRTGSVARPSGSELTDIGSGERCGNDRLTDSIGTIGGW PRGACLTWLKTKLPVMGAFLILSIIGWIVLGWA JM 138 MMDRIRNAPMTGSFVFSQVRQAPRGHPPIVPMESVNRSLPHRSPLPI SEQ ID NO: SVNSDPEGRATEPVRLNAPRPSECPVRAKTVLRRVFNRLALFGVTTK 139 NCKTCRCSVK JM 139 MSGDDLLAFESLLPEDMKIMFPTIYSRLNAINYCQYLKTFLCNRAQT SEQ ID NO: RSAHCEHCMVLDAKVNAVKQVIHKIVSTDAVFTGAAHST 140 JM 140 MFVPWQLETLMKHWPSLRELVEQSFLPGTPDVAFNSPVLIHTQDSLQ SEQ ID NO: PASSCRVCNILFTLVRTFPPPDSFFEDYGWLCLTCLYAPRSWTATLM 141 VAADLLELIHMYFPQRVKDGPVYTTQNILGIDVQLHFFATRCFRPID REQILHTSHLNFLQTEFIRGMLEGTIPGSFCFKTSWPRTEKDDQQPT VACCSVGRGNHANRDNHLPDDLEEAFNSTNAKEKPSILGVFSATWSE SQLLGSDTQQATIHSQPSTFPTPEDADQSQGPCLMHPTLNLKTKNHT ASICVLCECLAAHPDAGPVLRDLRRDILENNENNVKLVNRISYILND PDSLSHVRDEHLRGLIKRCSAQEIHKHFFCDPLCVLNTYSHCPAVLF KCPPPEKYKKLKARLATGEFLDCNRIFDCETLQTLAVLFKGSQLAKI GKTTSLEIIRELGFQLRRHNIQITHPFQTSNLYI JM 141 MYDMRLTSLTLFSMFSRMSRRRSLRTGPASGWAARHSHRTQMDAVWF SEQ ID NO: FVLRLSVGCIRQGPCDWSASSGVGKVEGCEWIVACCVSEPRSWDSDH 142 VAEKTPRMLGFSLAFVELNASSRSSGRWLSRLA JM 142 MFDECPNDERDTHRPGAMVFRFNGNITDFEVHIGVPISLKKSTPSSW SEQ ID NO: RRVRAEKMCVSETNFFHCIISLLQLPCLDAGCVDWGPSGRLTLGAYG 143 VRDANRRLGCFGIV JM 143 MPKQPRRRLASRTPYAPSVKRPDGPQSTQPASRHGSCKSEIMQWKKL SEQ ID NO: VSDTQFFSALTRRHELGVDFLREMGTPICTSKSVMLPLNLKTIAPGR 144 CVSLSSFGHSSNMGFNCSSCTPTDRSAVSLDANALGEDSARKNSELC SVALTFYHHAEKVVQHKGFYLSLLSHSMEVVRRSFTQPGLLYAHLVL KTFGHDPLPIFTVDANERLALWAVFHTRDLHLGETSLRLIMDNLPNY DITVDCIKQTYIMKFTPSRPDNATVTVPVNSICEAVATLDCTDEFRE EIQRGTTIINSQGSL JM 144 MLTRAPRLGASVQLTAVRLLLLFLTSSTPTAINCTKPGSVFFWLSWP SEQ ID NO: KVFMENHYSFISVNSVSITVVAAGKISSRGKTATNC 145 JM 145 MWCLVQRAGPPVGCRSPGGVQVPRWGAGPPVGCRSPGGVQVPRWGAG SEQ ID NO: PPVGCRSPGGVQVPRWGAGPPVGCRSPGGVQVPRWGAGPPVGCRSPG 146 GVQVPRWGAGPPVGCRSPGGVQVPRWGAGPPVGCRSPGGVQVPRWGA GPPVGCRSPGGVQVPRWGAGPPVGCRSPGGVQVPRWGAGPPVGCRSP GGVQVPRWGAGPPVGCRSPGGAPGGSGWGGGSGWLRVGWRLRVAPGG VAAPGGSGWAQVLKATVNPTANPTQKSPCASRAEARLLTCASGALYI GQNTLPK JM 146 MGNPRIDRSHSKHVGFTLFGESPLAGPNVPAPCTWVLRNAKLPLPCR SEQ ID NO: VPYSCSATFEYTALHGWRAVGRWCANQKLMIHLLVLWLHNNTMLLIL 147 GGCFGLYKGRRKHR JM 147 MYSWGEFRTMERKMSLRVTRGSQKHITMGLFGAHKRAVGNGLGGAPA SEQ ID NO: PPCARNLGRGVRRGSPKHVLMVAARTHRPLFGAGVIRRSAQNVAHGT 148 HCTHGAHEGGGVAGRSHRAGRGARRLWHRASDVYGRNPLSRGIKGRR QGRFPLARRAVNQTDARRRLVVATVGFLLRCRVPSRDWLGDLSIKNA RRPLAQPPVNIHGILAANWPKQTANPRVGFCLQVPLYYIYSIIFFPC JM 148 MTPAPKSGRWVRAATIKTCFGDPRLTPRPKLRAHGGAGAPPSPFPTA SEQ ID NO: RLWAPNRPMVICFCDPRVTRSDILRSMVLNSPHEYMFR 149 JM 149 MVPFGAHGAVFAARGRRRVTETCTHGANSGPWSAKCRSGSPEGHRNI SEQ ID NO: SPWAYLVPISGPWEMGSVGRRRHHVPAIWGAGSGGGHRNNF 150 JM 150 MSCEHFPPGYNGQESAGKTSTGLPVGEREARRYAACVSEVAPMGRMT SEQ ID NO: TPATRRAAGADISQNRPRRQAARLPPPTTLILAFKLLFKARLFVAPA 151 JM 151 MFPHKRIVDLGRHLEADDREAVLWLFDRPVSDNTPEGFANGLCPPTG SEQ ID NO: EPGIPFPVLLEAVFLVGRLDLVSTFFLLDVGFIVERLRSSPSYFSPY 152 KHLMLSINRQLSERDVKNLVFLTGNQLGRKRNQSPTFFQWISQMEKA ALVSPSDYLVLKDLLQAVSRRDVAKVVAANAPG JM 152 MAFVGPVPTGTIDPVLYQDRAISNLLAHETSFVTSTACYGTVQTEVT SEQ ID NO: LGMRVILGTWMRSVARAHQADASVFPLAVSILDRYLECRSIPRRRFQ 153 RLGAACLFLAGKIRDLNPFKAAFLCFCAADDFSVADLLKQEKSVLKA LRWKLEAVLPTDAIGPALFKSGFTKEQLFALHSRVVESVHKAIVNPV TGGLSPSLVAAACALFSLGAAAPPLDKLAEAIGVSAATLTAAAESVA TTLRELDEDRILNNARGSS JM 153 MWGSRQHRSGIVSGHGLRSSCRGHCGRRGGTREQAGGRSRGRGRGAA SEQ ID NO: APASASAASASPTPPGPQVLVVVEQGHGSDTETATESGHGSSQGSPS 154 GSGSESVIVLGSPTPSPSGSAPVLASDLSPRNTSGSSPGSPASHSPP PSPPSHPAPLSPAPPSSHHPSPDPQPPSFLQPLPHDSPEPPGPPTSS PPPNSPGPPQSPTPTSSPPPQSPPDSPGPQQSPTPQQAPSPNTQQAV SHTDHPAGPSRPGPPFPGHTSHTYTVGGWGPPRRPGGVPCLRLRCTS HNSHEDEVPERQREQEGEERQQQPARPPRPPRYPIPIPYPHPRRRYQ ENTAHKEDFIVRRWETGSTPLDRARGVTESSFVTQTPIHCIAWQGAY SFPGLEHPASAFCRTHLEVPSSRLFASRCSVKVAEPPRPSKKPVAGG NNFTHPPPTSMLA JM 154 MGPVEALAIAVVQVSRAGIAEGARTLALAIVVVQVSWEGARTLEAQA SEQ ID NO: VQVSRGATVAKTTEAADRAMDDATTAVQVRGGRGAMGVMVGANAMRG 155 IPGTTLMCFEVTGLKLTPAQTRLAMALEIPTR JM 155 MTDSDPDPEGDPCDDPCPDSVAVSVSDPCPCSTTTRTCGPGGVGEAE SEQ ID NO: AADAEAGAAAPRPLPRLRPPACSLVPPRLPQCPLQELRNPCPDTMPE 156 RCCRLPHMIAVYCV JM 156 MRARPDQNSPPPSGHNRKRTKHRFCVRALRWLRVVERAIYLICRFLH SEQ ID NO: AVNRDHVGQPATSFRHSIGTRVAKFLQGTLRKTRRH 157 JM 157 MALRVGGNLFEKDLLPPGVKHRHRPCVFNHVGRNYINAAAGDARHGS SEQ ID NO: VRSSNALCGGPRALYRVPWVRVNNSPQRSYRYLAKTGIA 158 JM 158 MLGGITLTLLLATLATVRCALQTHYAAVPVHSTASLGCVLTTAHNVL SEQ ID NO: IVTWQKQESPSPVNVATYSSEAGTVVQPPFAGRVDIPEHKLTRTTLK 159 FFNATMEDEGCYLCIFNAFGVGKLSGTACLTVYVPLSMSVTFYPPIN PTQLVCRAEASPAPSVNWTGVPPELCSEPEVFPRPNGTTLVVGRCNV TSVDPEDLRNATCLVTHIGGLASARPLGPVFSDPLEGTSHYVVGVVA AVAVLGIFLTGVFLYRSM JM 159 MSDQARGVSEVFGIHRRYVAATHDQGCSVGSGKHFGFAAQLGWHAGP SEQ ID NO: VNRRCGTGLGPTDKLRRVNWGVKRDGHGQGDVNRQAGGSRQLSHSKR 160 VKDTQVAPLVLHSGIKKLQGCSGQLVFGDVNPTGERGLNHRARFGTI CGHVNGARRFLFLPGNDKNVVGCC JM 160 MDALNNNLNLLMDFLSNYSNSYSSYDDNISYTLDTESTLCRLTIIFP SEQ ID NO: PTIYAIICFFIFCITLLGNALVLYIFFKFKALANSVDVLMAGLCCNS 161 LFLCASFLFSWLLYVAPQILTPATCKVEIFFFYLYTYFGVYIVVCIS LIRCLLVVFSRRPWVKHWASGFLCVCVSLIVALALSANASLYRTALR HPETSEWICYEDAGEDTVNWKLRIRTISAICGFLVPFGLLVLFYGLT WCIVKSTKLARKGAVRGVIVTVVVLFLIFCLPYHLCNFFDTLLRTGF VTETCYIRDVISVAMHICSLLQSMYSAFVPVVYSGLGSLFRRRVRDT WSMFRCFSTSGSL JM 161 MAQRTNPRWAAAALSADEEAFIHDNSDAESVLALVPEQCFSEFLLWL SEQ ID NO: VTRPSDNFDNDDDDPTLGVIWQLLAPLVNYAPLETRSAHLQGHHTIS 162 LPYGPDLLRQPTTRSSELVQCLRDSGFDTALRLELARHLSCQTRRFV ADRVPPGTFAALTLGALVEYDVRVQRQLPVTVQSTAWRPLPERDPIC AAVMLPLQRNILPLAVQASNGNSYTVSRYAVMARRSYGCVFQRLPCE NVTHIADSFTHLHSAIRTGAGALQDILFHSTLLPGGDIRSALCGFYA TTPSVGAFSRARHRAINTTTTLHCQQLARTGTPVLGGFLKTVHSATT SEANVITTTSLLSCVPQAYTFLRRSLFNQPIICLGSFEPVDGDGNQR SLYLGSAAGINRINQTLSLAYEILEGPLFTSINRAHEPASTISHLGA LVSRGGLRLFVSQLPPTILSQLTATPDISRETVNDILLNKFLNVSAF VVFAVLPRDTEPEPGPLDAIRRAARICGCPFAVVGETCEEPGIQFVN DLELWNPGAWPIRQPTSAEVIATFGFDEQPVSSNWLVRPEEPEEGGE QAPSPTDWGLFRLASVVDQLLRCPTVGSKEFVTRHVDRCSNGLVAQQ CEVGPLGRPLSDYHIVNHTAVFTDRMARVPIHRPQPITRQDATERLG SPETWVTQGRGRLRWVGQCVAHGEQAYKMGIDAAVGARYAICEAVTN IMLAHVRRLSDITLTASVGWNPEEDQAWLLQHALFACKELCRDLSVN FAITSAGSTPCLSEELISATQQHQTVAPVPFNAVIITATAEVKSSRR RVTPDLKATGNLLVLVTFPGPHLTQGSTFEHLCLLPSPTLPDVQATH LANLFMLTESMLSRGLVVSGHDVSDGGVVVTAIEMALAGNRGLQICI PSEETPLPWLVSETPGVIFEILPQHVDEVRQACQNFDCQATVCGTVG QEGLSERIVISHNNEEVYSQTLTSVAANWTSFSDEQWYSWGPSFTPA QELYRKDYGCNRHNLGHLADVCRNSELTLFAVPSRPPAVAALIAPGA PLPRALMPAFTNVGFDVAAVSTNDLRGGNILRGFSGLTIGGNVGIED SYVGARCAIMGLLNDPGCYGGLMAFFRRADTFSLCCGEFGFQLLGAL GLLRETPHDTPGPKTPDQWDIHLEENASGNBECLWLNLHIPQTTISI MFRVLRGLVLPGWANGRYLGVRYPRDAIEYHLNQQQRIAUJFHTGNP DPRMFAQHYPRNPSANSAVAAITSPDGRHLASLVDPAVVFHPWQWAY VPPELADMTISPWAIJAFQSLFLWCVRNRQ JM 162 MRNHGSSQRPWVLWGPYGILPPSGYIFTVLRGVWVPAPGGARSTQRN SEQ ID NO: PSRHAPAQNPRPVGHPPGGERIREPRVPLAKPPHPPDHHQHNV 163 JM 163 MPTFPPMVKPEMPRRMFPPLRSLVETAATSNPTLVNAAISALGSGAP SEQ ID NO: GAIRAATAGGLDGTANSVSSLFLQTSARWPRLCRLHP 164 JM 164 MTILSDRPSWPTVPHTVAWQSKFWHAWRTSSTCWGRISKITPGVSDT SEQ ID NO: SHGRGVSSDGMQICRPRLPAPAISIAVTTTPPSLTSWPDTTRPRESI 165 DSVSIKRLARCVA JM 165 MAKFTLRSRHSSLQANSACCSSQAWSSSGFQPTDAVSVMSLRRRTCA SEQ ID NO: SMMLVTASQMAYLAPTAASMPILYACSPWATHCPTHLSLPLPWVTQV 166 SGLPRRSVASCLVIGWGRCMGTRAILSVNTAVWLTMW JM 166 MPFCRRRGNLRRAGNPVRERPRAVEPGSVADQTADLGRSDRNFWVRR SEQ ID NO: AARFLQLAGAPRRTGGGRRTGTLADRLGPIPPGLRGRSASAMSNRRQ 167 QRVCHATCGQMLQRTRSSAVRSGTPGPTAVRLPHRQPHGGVYGQNGA GAHTSPPTDHQAGRDGTPG JM 167 MFRCNGSITAAHIGSLSGNGLQAVDCTVTGSWRCTRTSYSTSAPSVR SEQ ID NO: AANVPGGTRSAThRLVWQLRCLASSNRNAVSKPLSLRHCTSSLDLVV 168 GWRSRSGP JM 168 MFVSFATMGNTYDFYNNNIMEWTLQNYTLNTANIYSNGILWICMVKF SEQ ID NO: TNKHCKNNWIVVCNTCRYVAILLLFIINRGNIYEEINCLFFVTALIG 169 MYAVTEASTTSSLTMALAYSIITANTGIF JM 169 MACNCPFFVWCTWLFSNILTGTFWLISLAQYACDNNKDLYIVAVSTV SEQ ID NO: ACFFFLWKSLGLYFYQSRSQRLNTPLLKLIPWITGMTL 170 JM 170 MPGGGRPASGAARRGLWGPGLGGRRGAAPPGSAGPGRSRESAGPGGA SEQ ID NO: GPGGGPGPPRDPRPREPKAARRAARGGRGRRPRARAGPAEGREPGEA 171 GGAPLGGPGAARETLAPGARWRPRPRAAAGRAPGGPRRAPPLGALAW RRC JM 171 MPGGRRPAWRSSAGLPSPTSPRKVVSAPPGGGLGPGAPRRGRPRGAT SEQ ID NO: EGPGRTGDRENARGGGGQRGTCACLWNTMACWPARLLGSLQACC 172

[0227] Several JMHV ORFs have been identified that can impact this model system.

[0228] For example, JM25 is homologous to collagen and myosin. Collagen is found in the arterial walls and during MS disease there is a break down of the blood brain barrier. Some forms of myosin are found in neurons and is involved in vesicular transport.

[0229] JM26 is homologous to myosin and sphingosine kinase. Some forms of myosin are found in neurons and is involved in vesicular transport. Sphingosine kinase is involved in cell cycle progression and is a major component of oligodendroglia. Oligodendroglia is the non-deural cfells of ectodermal orgin forming part of the advential structure (neuroglia) of the central nervous system; projections of the surface membrane of each of these cells (oligodendrocytes) fan out and coil around the axon of many neurons to form myelin sheaths in the white matter. With micorglia, they form the perineuronal satellites in the gray matter.

[0230] JM39 is homologous to succinate dehydrogenase. Succinate dehydrogenase is found in the mitochondria and is an enzyme of the oxidoreductase class that catalyzes the oxidation of succinate to fumarate, using a variety of hydrogen acceptors. Succinate dehydrogenase is down regulated in patients with multiple sclerosis.

[0231] JM41 shows homology to alpha-1a adrenergic receptor. Adrenergic receptors are involved in secreting epinephrine or related substances, particularly in sympathetic nerve fibers that liberate norepinephrine at a synapse when a nerve impulse passes.

[0232] JM48 shows homology to mucin. Mucin is defined as any group of proteins-containing glycoconjugates with high sialic acid or sulfated polysaccharide content. Lipmatosis is a condition characterized by abnormal localized or tumor-like, accumulations of fat as well as an accumulation of mucin in the tissues. Lipomatous metaplastic changes occur with people diagnosed with multiple sclerosis.

[0233] JM54 is homologous to collagen and myosin. Collagen is found in the arterial walls and during MS disease there is a break down of the blood brain barrier. Some forms of myosin are found in neurons and is involved in vesicular transport.

[0234] JM57 has homology to calcium channel proteins. Mitochondrial calcium membrane potential is a component of cellular survival. Once membrane potential is lost a cell will progress towards apoptosis.

[0235] JM71 has homology to a chromatin associated protein. Chromatin is a deoxyribonucleic acid attached to a protein structure base and is the carrier of the genes in inheritance. A characteristic of apoptosis is chromatin condensation and DNA fragmentation. Therefore, JM71 may have an anti-apoptotic function.

[0236] JM76 has homology to plexin. Plexins have been shown to promote axon repulsion. Recent evidence has shown that if plexin expression is inhibited in carcinoma cell migration and when it is overexpressed migration is inhibited.

[0237] JM80 has homology to NADH-ubiquinone dehydrogenase. NADH-ubiquinone dehydrogenase is a protein involved in the mitochondrial electron transport chain. Generation of reactive oxygen species is a byproduct of this pathway and is important in the aging process and in neurodegenerative diseases.

[0238] JM85 has homology to a chromatin remodeling complex protein. Chromatin is a deoxyribonucleic acid attached to a protein structure base and is the carrier of the genes in inheritance. A characteristic of apoptosis is chromatin condensation and DNA fragmentation.

[0239] JM87 has homology to mucin. Mucin is defined as any group of proteins-containing glycoconjugates with high sialic acid or sulfated polysaccharide content. Lipmatosis is a condition characterized by abnormal localized or tumor-like, accumulations of fat as well as an accumulation of mucin in the tissues. Lipomatous metaplastic changes occur with people diagnosed with multiple sclerosis.

[0240] JM88 has homology to neurexin. Neurexins link the pre- and postsynaptic compartments of synapses by binding extracellularly to post-synaptic cell adhesion molecules and intracellularly to pre-synaptic PDZ domain proteins. These proteins are essential for Ca2+ triggered neurotransmitter release.

[0241] JM132 has homology to c-myc promoter binding protein. C-myc has been shown to be involved in cell proliferation and tumorgenesis.

[0242] JM152 has homology to cyclin D. Cyclin D is a key regulator of cell cycle. Cell cycle events that are regulated by cyclins play a major role in the loss of neurons in diseases such as Alzheimer's disease.

[0243] JM166 has homology to collagen. Collagen is found in the arterial walls and during MS disease there is a break down of the blood brain barrier JM167 has homology to myosin phosphatase. Some forms of myosin are found in neurons and is involved in vesicular transport.

[0244] JM168 has homology to a CC chemokine receptor. Recent evidence has shown CC chemokine receptor expression by mononuclear phagocytes in multiple sclerosis lesions.

Example 3 Non-Human Primate Model for MS

[0245] MS is a devastating disease affecting an estimated 1 million people worldwide, or 0.1% of the U.S. population. Current research is directed at elucidating potential viral/bacterial causes of MS, as well as determining the involvement of the host immune system in the disease. Rhesus macaques have provided a nonhuman primate experimental autoimmune encephalomyelitis (EAE) model of MS since the 1930's (Ferraro and Cazzull, J. Neuropathol Exp. Neurol. 7:235-260, 1948; Rivers, and Schwentker, J. Exp. Med. 61:689-705, 1935). Recently, the common marmoset has been used to develop an animal model for MS (Brok et al., J Immunol 165:1093-101, 2000; Genain and Hauser, J Mol Med 75:187-97, 1997). The marmoset model relies on myelin oligodendrocyte glycoprotein-specific antibodies for demyelination (Genain et al., Nat Med 5:170-5, 1999; Genain et al., J Clin Invest 96:2966-74, 1995; Raine et al., Ann Neurol 46:144-60, 1999). While EAE studies have provided data into how anti-myelin T cells and antibodies can cause demyelination, there are questions about their relevance. Even more important is that EAE induced in these animal models is due to active immunization with myelin antigens or passive transfer of myelin specific T cells, neither of which occurs in MS.

[0246] Until now there has not been a nonhuman primate model in which a naturally occurring chronic viral infection results in an MS-like demyelinating disease. The availability of the complete JMHV sequence, the ability to grow JMHV in vitro and the association of the virus with a demyelinating disease in vivo can be used in a relevant nonhuman primate model for MS in the Japanese macaque.

[0247] It will be apparent that the precise details of the methods or compositions described may be varied or modified without departing from the spirit of the described disclosure. We claim all such modifications and variations that fall within the scope and spirit of the claims below.

1 172 1 131217 DNA Japanese Macaque Herpesvirus 1 cccggggcgc gaccgagggc cccgggagaa cgggggatcg ggaaaacgcg aggggtggcg 60 ggggacagag gggaacgtgt gcgtgcttgt ggaacactat ggcctgctgg cctgctcgct 120 tgcttggtag cttgcaagct tgctgctgag ggtctttaga gggacagtag gcctgcttgc 180 tggcctgctt gctggcctgc ttgctggcct gcttgctggc ctgcttgctg gcctgcttgc 240 tggcctgctt tgctggcctg cttgctggcc tgcttgctgg cctgcttgct ggcctgcttg 300 ctggcctgct tgctggcctg cttgctggcc tgcttgctgg cctgcttgct ggcctgcttg 360 ctggcctgct tgctggcctg cttgctggcc tgcttgctgg cctgcttgct ggcctgcttg 420 ctggcctgct tgctggcctg cttgctggcc tgcttgctgg cctgcttgct tgctgctgag 480 gggacagtag ggctgcctgc ttgcttgctg ctgaggggac agtagggctg cctgcttgct 540 tgctgctgag gggacagtag ggctgcctgc ttgcttgctg ctgagtagga ctgctagggc 600 tggtagtagt ggggcagccg gccagctgcg tgcgagggcg ttgcagggcc acacgaggac 660 acgggacccg agccctcccc aggaccgccg ggcaagcggc ccagatctgc ccggcaggtc 720 gctcggggag agcggacgga aagggcggtg ggggctggga gcatagacgc ggggctggga 780 acggggagta gggggatggg aaggggtgca gacgtggggc cgggggacgg ggcgtggttt 840 gagaccccaa gctgatgact caaaaatggg ctaaaccacg cccacctcat ttttttcccc 900 cggccctatc ccaagcaacg ctcccccaac taaaactccc tcttgtcggc agctaagggt 960 cgcctgcctt cttcccattc cccacccatc cgctacaata aaaccgcctg cctgccgctg 1020 acggaaaaag gggaggtgtg tgtatgcttt tgtaactttc cagcggaggg ggtagagtgc 1080 acggccaatt tccaagcacc tgcttaactc gctttggctt tatgtggttt tgttgctatg 1140 tactacacac agtaattcat tgcatggcgc ctgcatacgc tccacagcat ccgaaacaag 1200 ttcatttctc tagactaact ttagtgttct tgttggctca taccatttta caaagtttgc 1260 tcctttgaat aataagaaat ccgttgtggt tacaatacac ctgccaatgt attggatggt 1320 ttcttttagc atagaccttg acttgcattt taacattgat tttttcccat tagaccctcg 1380 tttcttcatg caattaggta tgtctttgcc tgtgtttact ttgctctcct ccgttctgtg 1440 gaaatgtttg tgttgcttat atttatctta ttgcaacctg cgtcgttgga gcttttgccc 1500 gcaaaattaa ctgctgttcc aacgtggtgt ccaccgcatc ccggagatac ctacttgcta 1560 acctgccgcg gaacatctac ggccagagac cagcgcagca cacaatggtt tcgcaacaac 1620 acgcttatgc atgggagtaa tttctacggc aggctggtat ctgtaactcc caattctaca 1680 atatctgact ggtatgcgtg tcaaacaaaa acaacaacgc ggagcaatag catcgatttt 1740 cgggtaaggt catcgcgcct cacgctccaa gaacgttgct cttcatacgg ctattctaac 1800 gcaaataaca caagggtatt gaggtgttac tctggtggaa acgtaacttt aagaaacgtt 1860 gtttttcatt taaatggtac agcggtcatt aacggtacta caacagacat atatacattt 1920 gttttaacgg aaaagacagg cggaacatat tactgttctg cgtttattgg gactgaaaaa 1980 ctctattctc aaaaaattaa tgtgtttttt acttcattta cctttaaaca tacagacaat 2040 gttcaaaatg ggtcagaatt taataaaact gagcaaattc aacaaacagc taatgtacaa 2100 cacactgcaa actacgttgt gttctctgtt cccgtttttt ctattggtgt tttaacaggt 2160 attgcaatat cgttgattat gtgttggtta tttacgttgc gctgcaacaa gaactctgaa 2220 tcctcgaata ataggcatgc acaccaaacg agctacattc aaccctccca taatcagcat 2280 tcccatacaa gtgaaagtac tacccatacc tatagaaatg atcatcagga agagagtatt 2340 gaagaactac caaaccaaca cacacgtaaa actaattctt gtcaaacagt tttacttgaa 2400 gtgaaaaatg tagccttcga tggaccacag gggaacttgc acaatacaaa cgacgaagtg 2460 atggaacagt atgatgatgt ggttgtagaa aatatagaac aaacatcata tgataataat 2520 attgaacaga tggactatag tgacattata cgccccaatt ttaattacta cagtggacta 2580 atattggaag aagttgatga ggttttttac aatgaactag caaatcaata tcatggatta 2640 atactggaga atttagatca cgatgagtac aaccatttaa ataaattaaa catgatagaa 2700 cagtatgatt ggttagaata agtcacttgt gggttattct taaaataaac aaaacataaa 2760 caacattaaa aaaagtttta ttgtgtaact gctttattta ttaacctttt ttcatatact 2820 tgaaacttat atttaattcc attttcttca aagtttgtgt ctttacctgg taattctgat 2880 aacatggtat attcggtaaa attaattgat gggaaaaata catcacaatc aaaactctcc 2940 ataatgcgcg taatatatag ttttaaagaa cactcgtagt taagaacact ctcataaaca 3000 gattttcctc caataaccca aaccgtgttt aattgtttgg ttagtttata ttgtctatag 3060 aaattaaacg catcgtctag cgttcttgct agaaagtgcg ctccctttgg tggttcacgt 3120 aattctctgc tcagaatgat gttaattctg ttcgccagag ggcgcttctt ttcagggatg 3180 gaaaaccatg ttcttttccc cataataacc acattctttt cacctataac cgatggcgta 3240 gaagtcattt tctgaaaata catcatttcg tttttaaggt acggccaagg catggttccg 3300 tttttaccaa ttcctaattg tttatcaacc gcaacaatac agttaactgt aatgtccatg 3360 gttttggttg cccctaacgg gtttaacaca gaaatatttc acttataaac aaatacccac 3420 gtgacatgta cttactaatg tgagtactta acataatata gttaacaata ttcgctttca 3480 cataatggcg ttgcatatat aagcgacgtg gacttgtatg tttttatgag attaatcatg 3540 ttttggttcc ccgttaccgt gtgctttgta tgccacttta tactggtaaa tgcgcaaaat 3600 gaaacaaatg ttacctgtga taagcctaat tttgatagat ttatggttgc aatggaaaaa 3660 aaagaaaaat acgtccttgg agataaagtt gaattaactt gtcggcctgg atatacatta 3720 cagggaaaag tttacgtgca atgccttcaa agcggaatgt ggactacacc aaacgcagaa 3780 tgtcatagaa aaaaatgcac aaattatgga gatattctaa acgggcaggt aattgtacca 3840 gattctgaca atgcttttaa atttggaaca aatataacat ataagtgcaa tacaggatat 3900 ctccttcttg gcagtatggt ccgcacgtgc ctgctaactg gtaattcaaa caccgttaat 3960 tggcaacccg ccgctcctac atgtgagatt gaaaaatgta aaaaacaacc ggatattgaa 4020 aatggcaaat actatccagt tcaagacttt tacaactatc tggaaacaat tacgtttacg 4080 tgtaataaag atttttctct aattggaaat acaacaacaa cgtgtatgac aaatggcacg 4140 tggagcagcc cggttccaaa atgtgaacag ataacttgca gcgcccctaa tattgaacat 4200 ggaacgctat tagtgggttc ttcgcgtgta tacaagcacg gtcaatctat taccattggt 4260 tgtgaaaatg gatttacctt aaatggacat aaaatgtgta catgtgaata ttcatcgtgg 4320 aatccaccgc ttcctacatg cgtgcctata aataagactg ttccaactcc atcggaagta 4380 cccagtccag ggaccaataa gcaggaaagg cccacaccag aaaatccaaa gtcccatgag 4440 tcggaaacta caacagaaac accaaaaaca ggaacccata aatcagaaac accatcaaaa 4500 aaaataccta acccagagac ccacaaacca accaccccaa aatctggaac atcagaacaa 4560 acaaccaata ggccatcaaa agcaccgtcg caaaatccac caatggaacc cccgatgagt 4620 aaatggaaaa ggcatgttgt gttagttctt tttgcaagtg ttgcatccct gttattcgtg 4680 ctcgttaccc tttattgttg ttttctaaaa taactttttt gttttcaaat gcaggttcgc 4740 caggcaaact cgcacgcatt aaccaatctg ccgaccgccg ttgattccgg aattaagttt 4800 acattattca aggttgtcaa taaaggtggt ttataaatat tctcttgtgt ttattgtttt 4860 gtgttaactt gttatagcta tcacgccacc ttgtggggct acattataga gcattattat 4920 tttcaacttt atactttcac gtcctatgaa tcatactcat ccacatcacg tggcatgcga 4980 ttgtggccgg gactgaaatt aacacaaagg gtacataatc catccaggcg gcacacatta 5040 gacgcggttt ataaaactaa tatcccatgc gccaacgatc actgtcgctg gcgacgctgc 5100 tagaaaaaca ttttaacgtt gtttagcaga attaaataac acgtaatggc atccaaaggc 5160 aacgccggac aacccctgga agataatcag gggtctcgtg ccccaatagg cgcttgcgga 5220 tacgtatacg cgtattcgaa acaagacttt cccttcgctg aggcgtcaat actcggcaac 5280 aggccatctg gatctggcgt cttttcgtta cccatccttt acggacttac cgtcgaacac 5340 gaattccctc tcaccgtaaa agccgcacac aaaaaagttg acaccacaac gctcgccgtc 5400 aaggtgacgt gctttcacag agaggttatt gtttttcaca acgcaaacct attcaggccg 5460 gtgtttgaag gcaccggtct taacgaacta tgcgaggaag ccagggctct cttcgggtat 5520 acgcagttta tagaaccggg tccacctcac ggcatatgga accctctgga atgtccgcag 5580 ttaccggaca aggatgagat gttccttggc gttgtcgtga cggaagggtt taaggagaga 5640 ctgtggaggg gctgtctcgt tcccgcagtg tttcagaccc agcaggtgca gatcgccggg 5700 cgtcaggcgt tcaaagtgcc gttgtacgac gaagacctgt tcgcacctca cgggcatagg 5760 atgccgcggt tttaccataa agacgttagc gcgtacctct acaactccct ttttaccagt 5820 atcgcccagg ccctgagact caaagacgtg acggcggtca tccacgccac agaaaaacaa 5880 ttcatgcagg accattacaa aattgccaag atagtgcagg caaaacagtt ttccacgacg 5940 ctgccgaaaa cggcagacgg gtcgtcacac atgatcgtcg acagcgttgt tgccgagctc 6000 gcccttagtt acggctgtat gtttctcgag tgtccacagg acgcgtgtga gttgctgaac 6060 tacgatagct ggcccatatt tgacggttgc gactcatcag aggatagggt taacgcgtta 6120 gagcgctggt cggccgaaca ggccgttcac gtggcgggtc aactgttcgc tgccaattcg 6180 gtgctgtacc tgaccagagt gcaaaagcaa gcacccaggg gacaaaaggg agacgtgaac 6240 gtgtacaact cctttttcct tcaacacgga ctggggtttc tgaacgaggc gacgattaag 6300 gaaaacggca gcgaagcctt taagggcgtg ccctcaaacg ccctcgatgg ttcttcgttt 6360 acgccgtatc atctggccta tgccgcgtcg ttctcgcccc atctgctggc aaagttatgt 6420 tattacatgc agttcttgca gcaccacaaa agctccacga accaaacgtt caacatagtc 6480 cactatgtcg gcaccgccgc caactcagaa atgtgcacgc tgtgtcacgg cgacacgccg 6540 ggaacgtgcc tcaacacgct gttctataga ctgaaggata ggtttccagc cgtaaccacc 6600 cctcagcgca gggaccccta cgtggtgacc ggaaccgccg gaacctttaa cgacctggag 6660 atcctgggca acttcgcgag tttcagagac cgcgaggagg acggaaaccc tgccgacgag 6720 cacccaaagt acacgtactg gcagctatgt cagaccgtga cggaaaagtt atccgcgatc 6780 ggaattaccg aggaccagga taaccacgtg aacctcatca ccaacatcca aagttttctc 6840 agggtgttca agggtatcga ctcggtggtg gacggagagg tcatgaaatt tattaactcg 6900 atgattaaaa ataactttaa ttttcgcgag cacgttaaat cggtccacca catacttcag 6960 ttctgctgca acgtgtattg gcaggcgccg tgcgcggtgt tcctgaatct gtactacaaa 7020 tccctactgt ggatcatcca ggatatctgc ctgccgtact gcatgatcta cgaacaagat 7080 aatccggcga tgggcatcct cccctccgag tggctaaaga tgcattttca aacgttgtgg 7140 acgaacttca aagcggcatg tctcgaccgc ggggtcctca cgggatgcga actgaaaata 7200 gtacaccggg acatgttctg cgacttcttc gacaccgacg ccgggtccaa cggtttactg 7260 gcccccttta aaatgcaggt tagaatagcc agagctatga tggtcgttcc gaaatcgatt 7320 aaaataaaaa atagaattat tttttccaac accgcgggtt ccgaggcggt gcagtcggga 7380 ttcgttaaac caacgggaac cagggacacc tacgtagtgg ccggaccgta catgaaattt 7440 ctaaactcgc tccatcgcgc gctattccca aacaccaaga ccgccgcgct gtacctgtgg 7500 cacaaaatct cccagaccaa caaaacccca gtcctgaaag acgtcccgga cgacgagctg 7560 gcggagctgg tgtcgtacgt caaaaccaac agcctcgcgt tcgaggaaac gaacgtgctg 7620 gacgtggtcc cggattccct catgtcgtac gcgaggatta aactgaacgg ggccattctg 7680 agggcgtgcg gtcaaattca gttctacgcc acaacgctgc attgccttac gccggtgtta 7740 caaactatcg acgccgagga atacccccac gtgctaggct ccgcggcgat tgccacgccg 7800 gtggcttacc tgtccgaaat acgcggccgc accgccctca ccgtccaaac gacggcgcgt 7860 cagccggtcg ccgccacggg gcgtctgcgc cccgtgataa ccgtacccat ggtagttaac 7920 aaatacacgg gagttaacgg gaacaacaac gtttttcact gcgggaacct ggggtacttc 7980 gcggggcgcg gcgtggaccg caacctgtgg ccggaaagtt ccccctttaa gaaaacgggc 8040 gtcagcgcaa tgctcagaaa gagacacgtc atgatgaccc ccatagtcga ccgcctgata 8100 aagcgagccg cgggacagac gatcagcacg ttcgaggcgg agagcgtcaa aaggagcgtg 8160 caggcgctgt tagaggacaa agacaacccc aacctactga agtcggtgat cttggagctt 8220 atacgacatc tgggaaaggg ctgccaggac ttaagctcgg aggacgtgca atattacctc 8280 ggtgactatt gcatgttgac ggacgaggtt ttatttacgt tggataatat agcacagtca 8340 ggcgtgccgt ggacattcga ggacgcgggt gccctgatag aagatcgcca gaacacagac 8400 gatcttcagt tcgtggacag cgacgatatc gccaccgctt cctgccagcc ccccgaggaa 8460 cagctaccga cccctagcgc cggcgcccta ctggccggga agaagcgtaa aattaacgtg 8520 ctactgagtg atttagacct ctaggaaaac cgtggtcggc gaacaacgat ggccagggaa 8580 ctcgcggcct tatacgcgca gctgtcggcc cttgccgtcg atctgagtct ggtggtcttt 8640 gctgacccgc gaagtatcga cggttcccgc attctaaaaa caaaaacaca gatagaaaac 8700 ctgaaccgcg acctcctgcc gctactacgc aagcaaaact cggtagagac gtccagcctg 8760 tcgctcgaag tggagcacct ggccaaaaac atcgaggaca aactcgggga gctagagcgc 8820 agtttgcggc aaagatattc gagccgagag cattttgaga cactacacct gaggcccgag 8880 tgtcactatc acgctacggt tacctttgag ttttacgggg gtgggctaat agatgtaaac 8940 atgtgcctaa taaacgatgt agaactgctg tgtaaaagac tagggagtgt gttttattgc 9000 atcggtgcga acgaagccct gtccggattg gaccgggttt tggcgtttct gtccacactg 9060 cggggtatct cccccatccc gcacccagac ctatacgtca cgtccgtgcc ttgcgtacag 9120 tgcctgcggg aaatcgaact agtaccaaat caggggtcca gtttactcgc ggtgttggca 9180 gaccgacact gcgatcacct ctgtaagaag gttagggcgg agccaataca cggcctgttt 9240 gagacagaac tcagccagtt gggtctaaaa gtagcaaaag gttcggacgc cacgcagcac 9300 ggcgtccggt cctcggcaga tcagttaagg gagtcgtcgc tggcggccat acaagatcac 9360 aatatattca agcgggtgtc cgcgtcaatc atggaactat ccaatctaat ttattggaac 9420 gccgggcaaa ccggcctcca gaccgggaca gaaaacgagt gctcccaaat ggccaaactg 9480 ctaacacacg aggccgagat gcacgagcac cgtgcgctaa taacacccaa acaaagcgcg 9540 gctcacttct acgactgttt ccgaccggat cccatagagt ccctgttctg cggcggtctt 9600 tttaactcta tagacgatac cattaacgca ctgagccggg attgttcggt aacgttcttt 9660 caacaggcaa actataccaa cgtcatgcga aaacaaaacg agctgtttac cagactcaac 9720 agcatattgt gtcaggggag cgcgggatcg caaaaaccgg ccaccccctc ggagccacgg 9780 accgccaccg tcgcggcgac cgcggcaagc gacgtcatta aagacgcaca atatcgcaaa 9840 gaacagtaca tgaaaaaggt ggccagggac ggctttaaaa aactaacaga gtgtctgcag 9900 acgcaaagcg cggtgttggc aaacgcgctc tgcatgcgcg tatggggggg cgtcgcatac 9960 ggcgaggcgt ccgagctggt gaaccatttt ctcctcaggc ggcgcttcgt cgcgcttccc 10020 tgggaagcgc gctgccgctc gaatcagatt ttattcgaaa actcaaagta cattaaaaac 10080 tcactatatt cccagcgcct cagtcgcgaa cacgtagaga ttatcacact gcagttttac 10140 ggcctgataa ccggccccct aacgcgccag agcgatctct ttcccggccc cgccaacgtc 10200 gtgctggccc agtgtttcga ggcggccgga atgcttccgc atcacaaaat gctggtgtca 10260 gagatgatat ggccccagat tcaaccgaaa gactggatag accagacatt taatcgtttt 10320 taccaacttc ccgaaggtga tctcaacgcg gtacaaaagt ccgcctggtg cttcatacga 10380 gagctcgtcc tctcggtggc gctttataat cgcacgtggg aaaagacgct gaggatattt 10440 tccctggcgc gcgagaaacc ctccatctcc gacctagacg ttaaaagcct gacgcccggc 10500 ctgtatctaa cgtacgagca aaacacgccg ctcgttctaa tttctcaaaa taccggctgg 10560 atatttaaag acctgtacgc ccttctgtac catcacctgc aactgtcaga cggccatgat 10620 gataactaac cggacgcgtc gtctgctgcg ggcgtgggtc gtgataatcg cgattggcgc 10680 ggcggttggc gaaaacgtca ccaccccaaa gggcgtgacc accactgcaa agtccacgcc 10740 gggcccgtcg acgcccacac ctcccgaaaa cccacccagg gccgaggcgt tcaagtttcg 10800 cgtgtgcagc gcctcggcca ccggcgaact cttcaggttt aacctggaaa agacgtgtcc 10860 tggcaccgag gacaaaacgc accaagaagg cattctaatg gtgtttaaaa aaaatatcgt 10920 cccccacatc tttaaggtta ggcggtaccg caaggtggcc acctcggtaa ccgtctatcg 10980 agggtggacc gagaccgccg tgaccggtaa gcaagaggtc attcgaccgg tgccgcagta 11040 cgagattaac cacatggaca cgacctacca gtgtttcagc tccatgcgcg tgaacgttaa 11100 cggcatcgaa aacacctaca cggacaggga cttcactaac cagaccgtgt tcctgcaacc 11160 ggtcgagggg ctcacggata acattcagcg atacttcagt cagccggtgc tgtacacgac 11220 accgggatgg tttcctggaa tctacagggt ccgaaccacg gtcaactgcg agatcgtgga 11280 catgatcgcg cgttcggcgg aaccgtactc ttactttgtc accgccctgg gagacacggt 11340 agaggtatcg ccgttctgct taaacgactc gacgtgctcc gtcgctgata aagccgaaaa 11400 cggcctcggc gtgcgcgtgc ttacaaatta caccattgtt gacttcgcta cccgcacgcc 11460 caccaccgaa acgcgagttt tcgcagactc gggagaatac accgtatcgt ggaaggcgga 11520 agaccctaag tcggcagtct gtgcgctgac gctctggaaa accttcccca gggccataca 11580 gacgacgcac gaagccagct accacttcgt ggccaacgac gtgacggcaa cctttacgtc 11640 cccgctctcc gaggtagcca actttactgg cacgtactcc tgccttgaca atgtaattca 11700 gaaaaccctc aacgccacca ttaagaagct gtctgataca cacgcggcaa acgggtcggc 11760 gcagtactac gagacggagg ggggactgtt tctactgtgg cagccgttaa cgcaactgag 11820 cctcgtcgac gagatgcgcg gcttaaatga caccacgccg gcacccccca ccacttcaac 11880 agccagtcgc gtgcgtagaa gcgtcgatac aaattcgcaa acggccgagg acctcgcagc 11940 gccacagctt cagttcgctt atgacaaact acgcgcaagc attaacaagg tgctggagga 12000 actatccagg gcgtggtgcc gagaacaggt gagggacacc tacatgtggt acgaactcag 12060 taagatcaac cccaccagcg taatgacggc aatatacggg cggccggtgt cggccaagtt 12120 tgtgggcgat gccatctccg tgacggactg cgtaacggtg gaccaagggt ccgtcagcat 12180 tcacaagagc ctccgcacgt ccacccctgg gatttgctac tcgcgccccc cggttacttt 12240 caggtttctt aacagcacca cgctgtttaa gggccagctg ggacccagga acgagatcat 12300 actgaccgac aaccaggtgg aggcgtgcaa agagacgtgc gaacactatt tcatcgccag 12360 caacgtaacg tactactaca aagactacgt atttgtaaaa aaaattaaca cctccgagat 12420 atccaccctc ggtacgttca tcgccctcaa cctgtcgttt atagagaaca ttgactttag 12480 ggttatagaa ctgtacagcc gtgcggagaa aaagctgtcc gggagcgttt ttgatataga 12540 aaccatgttc agggaataca actactacac gcaacgactg gcggggctcc gagaggacct 12600 ggacaacacg atcgacctga accgcgaccg cctggcacgc gacctgtccg atatagtcgc 12660 ggacctgggc gacgttggcc gcacggtcgt taacgtggcc agtagcgtga taaccctgtt 12720 cgggtctatc gtgagcgggt tcattaactt tataaagagt ccgttcgggg gcatgctcat 12780 gatcctggtg atcgtggcgg tcatcctaat cgtgttcgcg ctaaatcggc gcaccaacgc 12840 catcgcccag gcccccatta ggatgatcta ccccgacata gacaaaatgc agccctctgg 12900 cggtaaagtc gaccaggagc agattaaaaa cattctcgcc ggcatgcacc agctacaaca 12960 ggaagagcgt aggcggttag acgaaaagca aaggtcggcg ccctcgcttt tccggcgcgc 13020 gtcagacgga ctaaaacgtc gttttagggg atataaacca ctggaaaacg aagaggctca 13080 ggagtatgag atgaacaaat aaccacaccc atacgcctgt acttgccgcc cgccagagcc 13140 gcgcggccaa tcgattcgcg cacccggccg gtcccaacac cctctggcgc ccccgggcgt 13200 cagcgttctg tatcgagcat ggattttttt aacccgtacc tgggtcctcg aggaccacgc 13260 cccccctcac acaaatgcac cgatgcgccc gcccccgccg gcgccgttca gccgccacca 13320 gacgtctgca ggctcattcc cgcctgcctc cgaacgccgg gggcaggcgg gatgatcccg 13380 gtcacgatcc cgttcccgcc gacgtacttt gaaaacggcg cgcgcggaga cgtgctgctc 13440 gcccacgaac ggtccatgtg gacggcgcgc ggccaacggc cagtcgtccc ggacccccaa 13500 gaccaatcca ttacgtttca cgcgtacgac gtcgttgaaa cgacgtacgc ggcggacagg 13560 tgcgccgagg taccgagccg cttccagacg gacattattc cgagcggaac cgtgctcaag 13620 ctcctggggc gaaccgagaa cggcaccagc gtgtgcgtga acgtgttccg tcaacaggta 13680 tatttctacg cgaaggtccc agccggcgtc aacgtcaccc acgtcctcca gcaggccctc 13740 aagaacaccg ccggcagggc cgcgtgcggc ttctcgacca gacgagtaac caaaaaaatt 13800 ctcaaaacgt acgacgtcgc ggagcatccc gtcactgaaa tcacgctatc gtccggttcc 13860 atgctctcga ccctcagcga ccgcctcgtc gcgtgcgggt gcgaggtgtt cgagtcaaac 13920 gtggacgccg ttcgccggtt cgtcctggat cacgggttta ccacgttcgg gtggtactcg 13980 tgcgcgcgtg ccacgccccg cctagcggcc agagatgcca gaacggccct ggagtttgac 14040 tgcagctggg aggacctcag cgttcaagcg gaccgcagcg actggccccc gtaccgcatc 14100 gtggccttcg atatagagtg catgggagag gcgggattcc cgtgcgccac gcgcgacggc 14160 gacgcggtga tccagatctc ctgcgtgttc tacacgacca gggaaggcgc gcccaatccg 14220 ccaaacatac tgttcagcgt cggaacgtgc gaccccatcc cggacaccga cgttctggag 14280 tttccgtcgg aatatgacat gctggtgtcg ttcttcgcca tgctccgaga cttcgaggtg 14340 gactttttaa ccggctacaa catctcaaac ttcgatctcc cttacctgat tacgcgagcg 14400 tcccaggtgt acaatctccg attaaacgaa tacacgaaaa taaagaccgg ctctatcttt 14460 gaagttcacg aaccccgtgg cgggggaggg gggttcatga ggtcggtctc caaaattaag 14520 atagcgggca tcgtccccat agacatgtac caggtgtgtc gcgaaaagct cagcctctcc 14580 gactacaaac tggacacggt ggccaggcag tgtttaggcg gaaaaaaaga ggacgtatcg 14640 tacaaggata tcccccctct gtttcgctca ggtcccggtg ggagggctaa ggtgggcagc 14700 tattgcgtaa tggactcagt cctggtgatg gacctcttaa aaatgtttat gatacacgtg 14760 gaaatctcgg agatagccaa gctggccaaa attcaggcca ggcgcgtcct aacggacggc 14820 caacagcttc gcgtgttctc ctgcctgttg gaggccgcgg ccagggataa ctttatcctc 14880 ccggtcccaa cgcccgaggg acaggggggt tatcagggcg cgacggtgat taaccccatc 14940 ccggggtttt acgacgagcc ggtcctggtg gtcgattttg ccagcctgta cccaagcatc 15000 atccaggcgc acaacctgtg ctactccacc atgatacacg gacgagacct gcacctgcac 15060 cccaacctga cgccggacga ctacgagacg ttcgtgctga gcggcggacc ggtgcatttt 15120 gtaaaaaaac acaagcggga gtctctgctg ggaagactgc taaccgtgtg gctagaaaag 15180 cgaagggcga tccggcgcac cctggcggcg tgcgacgacc cgtcgctgaa aaccatctta 15240 gataaacaac agctggccat caaggtgacc tgtaacgcgg tttacgggtt caccggggtg 15300 gccagcggac tcctcccatg cattaacata gcggagaccg tgacgctccg ggggcgcacg 15360 atgctggaga tgtcaaagtc ttacgtggag gccctaacga cggacaacct gcgaacgcgc 15420 ctcggtcgcg aggtgaccgc ctgtcacggt gcgcggtttc gcgtcgtcta cggtgacacc 15480 gactcgctct tcatcgcgtg cgacggttac tccgcggaag ccgtttccgc tttctgcgac 15540 gatctggcag ccaggatcac ggcggacctg ttccccccac cgattaagct agaggcggaa 15600 aagacgttca agtgtttgct gctgctgacg aaaaagcgct acatcggggt cctattgaac 15660 gacaaaatgg ttatgaaagg ggtcgacctc attcgcaaaa cggcctgcaa gtttgtccag 15720 gagcgatgcc gctccatcct ggacctggtg ctccacaatc aggaggtcaa ggcggcggcg 15780 cggctgttgt gcaagcgacc gccgcacgcg gtatacgagg aggggttgcc ggcgggcttt 15840 ataaaaattg tggaggtcct caacgcgagc tatgtggacc ttcgaaacag cgtcgtgccc 15900 atcgagcagt taacgttctc gaccgagctc agccgccccg tctgcgatta caagaccacc 15960 aacctgcccc acctggcggt gtaccagaag ctggcgagca ggtgcgagga gctgccccag 16020 gtgcacgata gaatccccta cgtgttcgtg gacgcgcccg gggccctaaa gtcggacctg 16080 gccgaacacc cggattacgt caaacagcac cagatccccg tcgcggtcga cctgtatttc 16140 gacaaactgg tgcacggcgc ggccaacatc ctccagtgcc tgtttggcaa caacgcggac 16200 accacggtgg ccatcctcta caattttctc aacgtcccgt ataagctgtt ctcgtgaacg 16260 ccgatagaaa aacgccagca taaaacgccg cgccgcggag tttgtgggga aagctcgcgc 16320 ggcgaggaac gaccagcgga gaccgccacc atgctggtta acgagctgtc gatggtcctc 16380 ggcgactggg aggtgacctt tcaccggggt aaattcagct tcgtcaacct agcccgcctg 16440 cagacgttta agggccacgg gggctacgcc aaaatccgtc tccccttctc gctcgaccag 16500 ttactccacc aacacttcgc gttcggactc gtgacgcgtc tcaacgaact gccccccttc 16560 tccgactgcg tggccctcat cgccccacgg gattccggcg gcgacgcgga cgcggcgcgc 16620 gtggcccccg ggttcgtgct agactcctct cgcccgctaa ccgtgtgggt gaacgcgaac 16680 gggcggcaca cggtccggtt ctgcctcctc ttcctaaagc cgatcgacct ggagcgcgcg 16740 gttacgtacg tcttcggcga gaacggcggc gcgcgctcgg aaggcgcccc aaagcccaca 16800 tgcaataccg aaagcctgcc cggcggaccc ctgcgcgtct ccggcgaggc gtctcagacg 16860 tcgccccact ctttcgtcgc gtattttccc acggccgatc cggtggcctg cctgagcctg 16920 ttgcggttac aggtgaggcc gttttcggat gacgcggcac acagggacgc gcggatctcc 16980 ccgaaatacg tcacgttcag taacgccggg ggtaacgtct gcaaggcgtc cgttcacacg 17040 ctgtccccgt cgcggtgtaa aacggcgcaa atggaaatca tttacgctcc gggggacccc 17100 aacgccgaga tagtcctggg ccagtccgga cccgtcctgc ccacccacac cggcggccgc 17160 gtattggggg tgtacgccga cgccgaaaaa accatccaac ctggaagctc cgcggaagtc 17220 cgggttcagt taatcttcca acagggagcg gccgctcggg gcgatctggc gtttctagtt 17280 gcgggcgtgg caccggagcc cctattcatc gtcaccccaa cacttttgct ttccggttgc 17340 acaacacacc tgcgcctatt caaccccaac ggtaccccca cgactataaa aagagacacc 17400 ctggtggccg ccgccgcgcc ctgccccgtg gtgcgagtaa gctccgccga cgacgcgccg 17460 cgggatctcg tcgcgtcacc agacaccggg gcgctctcca ttgacgcgtt cacaatcccg 17520 gtcggtctcc ccggggtggt ctcggcggag tgtcacgtgt ctatgcgcga caacggggtc 17580 cacgaacgca tgagccatta acggcgacaa tgggaacacc ggtgcgtttc tttcgcggcg 17640 agtggcaaac ctcgagtctg gtggacaacg gcacgccacg gtacagctcc ctggtgtggg 17700 ccgccactat ccacgacggc tacctgacac tggtgaacag gtcggagctg tgcgtcacgg 17760 agcggtctcc gtgtctgccg gcgtgcccca gcatcgggag actggtcggg aagaggtttc 17820 ccggcttcgc ctttgccagc gccacgctgg gcgatcgggg aacacgcacc gtgttctacg 17880 cgttcggtca ccgcgacaac cccctggaca tcgtacccgc cgtggtcgag cgcgcggacc 17940 gcgagctggt gctgcgagtt cacgcgccgc gaacgacgcg ggtgtcgcga tacggactta 18000 agatatttgt ggcgatcgtc actgtggtgc gcccgcccgg ggtgtttcta cacttcccac 18060 aagaccgcgt tccgatagcg ctgacggacg cgtgcagcca ggagggctcc aggctaacct 18120 ctgaagagcc gtggataaaa attcaaggct ttcccgtcct gtcggacgag accgcgcatc 18180 cgtttctctt aacccagaag accaagccct ttaccgagcg caagttctgc cgcctgatca 18240 tggacgacaa ccagctcagc gccgtcaaca ccgtctacct gggaaagcag cacgtgaggg 18300 taaccgtgac ccgccccccg gaaacaatcg tcaccgacgg ccccgtaacg gcaaccctgt 18360 ccctcaccgg taatgctcca atcgcctttc gccacaaccc atactttgaa ctcccgtggt 18420 cgtccacgac ggcgatattc actcccgtgg tgtacgtggg cctgaccgtg tgcatcccac 18480 ccaactgtag caaatttgtg aggtacggta acacctacgt ctcggcattt aaccgcaagc 18540 tgacggcgat tattagcaac cacgcccacg acggcgggtt tcgcattcag gactgcgagt 18600 ggccaccgaa ccgggagata gagattttgg taaccaacgt aacccaggcc ccggtgtatg 18660 tcagcactgg aacgcagctg gggcgagcca tctttgtgtt cgcgccgcgg ttcggcggcc 18720 cggcaaaact gcggcagctt ctcggccacc gatcgcgcgc gctggagctg cctggcgggg 18780 taaccgtgga cagccaaaaa ctgtgtaggt ttgaaaccat gtacctgttt tccacgtaaa 18840 ttacgaataa accggtcgtt cgtattactc acacaacgcc aaaccgtctt tcattctcgg 18900 ggtcgcgcgt ttcgcaaaca cacgaggttt cccagacacc ccctcccgta ccctcgccac 18960 acaaagccaa agccagtcaa cggctttcgt taaatgcaga gtttatttat tattttctta 19020 catcatagct attgcgcggc gcccgtcccg caaaaacatc tgtagatatt ccagtagacg 19080 aaacgcgcta agaataacgt ccccggggct ctgctctgct aacgcgcgca caattttatc 19140 gttagactcc acgccaccta tcttgttatc cacgggcagc tcctcgatta atgagttgag 19200 ggcggacagc accacggtca ccgcggagcc gatggccgcg gcgcccgcgt ttccgggcgc 19260 gtcgtccagc agcatcttcg agcgcgtcag gtaactctcg taggcacgga gcccgcgaac 19320 catggcgttc atacactcgg ccccgcgaaa ctcgcggcgc tggcactcga cgttagacat 19380 taatataggg aagttaataa acgacatgat gcgcgggtac tcacgcaccc gacagagagt 19440 ggagtggtag cacaggtaaa cgaaccagcg ctgtatgttt aaccccagct cggacaagcg 19500 ccccctggtc cggtcaagag aggcgcggtt accggcccac tgggggagaa cgttaattcc 19560 agcggcagtc gggggaggcg ccagcgtagg gctggccgcc caacacgaca ggtaaaacaa 19620 gacgaaccag acaggaaaca taaccggtta aattactcgc tcacaatcgc gggcggcggc 19680 cggttaacgc caggtccata aaaacacacc tgccgccaac ccccaaagcg ggaccgcgcc 19740 ctggaacgcg gttccttcca atcgcaaaga accgcgtcac aaaaagggct cgtttggaac 19800 cccttttgtg ccagtttcca aagacggaaa cggctcgttc gaaaatacaa aacggggtgc 19860 tcaaacggcc atctccatct ctatgtgggg gtgggggtcg taaccctcga gactcaggtc 19920 cgcacgcgta aagtcctcca gacgcgtcac ctttctcaga atcttcaacc gcgggaaagg 19980 acgcggggtc ctccccagct gaagcagcag gggcccaacg tggttgttgt aaacgtgggc 20040 atcccccagg gtgtgtacaa agtctcccgg ggtcaggccc gtgacgtgcg ctattagata 20100 cgtcaggagg gcgtagctgg caatgttaaa cgggaccccg aggcccatgt cggcggacct 20160 ctggtacagc tggcatgaca gctccccccg agccacgtaa aactgacaca aaacgtgaca 20220 cggcgggagg gccatcctcg caaggtccgc ggggttccac gcgcacatga caattcgccg 20280 atcgtggggc cgtctgacga tcaggtccac cacgtagcgc agctggtcca ccccttgacc 20340 ttcgtagtct gcatcggccc ccctgtactc cgccccaaag tgcctccact ggaacccgta 20400 caccggcccc aggtcgccct cgcggcggtc cccaaagccc tgcgccgcca agaaggcgcg 20460 ggacccgtgc gcgtcccaaa tttttacgcc gcggcgcgac agttcggtgg agtcggtgga 20520 gcctctgata aaccacaaca actcctccac gacgcccctc cagaacaccc ttttggtggt 20580 caacagggga aactcgtccc taaggttata tcgggcctga agcccaaaca cggacctggt 20640 tcccacgccc gtcctgtcat ccctctgaac gccgtgtctg atgattaaat ccaggtgcgc 20700 caggtactgc agctcgccgt gctcgccgcg gccgtccggg gcacgcgccg cggcaacctc 20760 ggatccgcga gaaacgcgac aacgcacggc cgctattcca gacaagcaag cgggtataat 20820 ttttttaacg tagcagatac cgagatgcac caggacaatc ataattatga ccgaggcgct 20880 tcacaactac agcccgtaaa cggctgaaaa cgagtctcat tttaaaggca gcttgggcgg 20940 ggtcaggcca caaggcgcgg cccggctatt agcgagtagt aaacccacgt ggtccctccc 21000 cagcgtctcc cccagagtcc cccccggcgt ctcccccgga gtctcccccg gcgtctcccc 21060 cggagtctcc cccggcgtct cccccggagt ctcccccggc gtctcccccg gagtctcccc 21120 cagcgtctcc cccggagtct cccccagcgt tcattaacca aacacgcata gtacaggaac 21180 cacaaaatac gtttattttt agtgtcatcg tggaagcgcc cccgtggagg cacatagtaa 21240 tagagtgcga ttcggcatca cgcggaaata taaacggagg gtcggtacgt ataacgtcgt 21300 aaataagcag ttgcgcgttg cttgcaaatt ccagcggccc gcggcaagcg ttacgggccc 21360 aaccgcgttg gccccggggg tctttttaga aaccgctgcc agactccagg ccttcgtcgg 21420 aagcatcgtc aagcaggctg cgccgggttc ttctgccctt gttgcgcttg ggacgattgt 21480 ccaccttctg aagcagctta cgcaccccgt cgtccccggg attggcgcac agcttctgac 21540 cgcggtgggt ctctaatatt acagcatcca gcgtacactg tgacgaggta tagtagtaaa 21600 gggccacggc cccagaaggc ggcaacttat ttatataccc taaacagcaa acttcgggtg 21660 ccggtccgct catggagccc atgggaaagg cataatccac cacacacgca aacaccgcaa 21720 aaaaggcgcc aatcacaagg accctcatgg tgacaaaaaa cacaaaacaa cggagagaca 21780 aagttactcg tccgttacca ccagcgccgc gctcgccgtg cttggccacg gatgacggcg 21840 tccattaata cccgcggccc gggtccgcct cgacggaaac caggcgtggc cagccacctg 21900 gcgcacgtgc ctcccgtcca gatgtggcgt cgcgagtccc aaaacgggcg tgtctaacta 21960 cggtcgcccc cggggttcga aagaacgggg attccccaaa caggtaaaca gcttttcgcc 22020 ttaacagaga gccggtactg aaaggaatct ccaaaacaag caggggtccc gtgccagcga 22080 taaacgggaa atctccccca cctaaacaca cgcgccgcat aaactaataa aacacacaaa 22140 acttccccag cccgtgtgca ataaaaacac acaagggtcg tcatctcgcg gggcccaaag 22200 ggccccgcgc gtctgggggc gcgttgtctc gtcgtggctc gcaatcaccg ccccgtctgc 22260 ccgaaaacag ggaaaccacc ctcaggccta gtttttaaaa cttaacactg gcaagggaaa 22320 agggaggata ggcgcggtta aaggaaaagg gcaaccgccg ggtcagcacg ggcagcgagg 22380 ggcaccaacc ccaaaataac acaacgtgat agcgtaaaac cccgcgggcg ttccgcgtgt 22440 tttgcgggcc ggggtcggca cggccaatcc cgcgttgggc gttcgcacaa gcacgctttg 22500 ctccgcaccc aggcaggggg cgccacgcgg cggcgccggt tcaggggtca ccagtgggtc 22560 agaaaaaata gtttccacgg tcgcccggcg cgcgcgtgga aacatctttc ggtgccctcc 22620 gaacgacccg aaaaatcccc gccgcaccgg gtcgttcgga gggcaccgaa aaatatcccc 22680 aattgcaacc aagaacaaca tgtccggggt ttcggtgacg cgcggagcag aggcggccgg 22740 tggtggcgtc ggcaaaaata gtggccggag agcacgggtt tcggtaatga cgcgcctgga 22800 cggcggccac ctggcggcgg gccagagacg cgagcaccgc gagcggccgg caggtggcgc 22860 cgcgagagac cgagcgccgc gatctgtcaa gatggcggac cggcggcgcc gattgggcgc 22920 agcggacgtc aatcacggcg gagaggagcg ccgttggtcg ggttacacgt caatcaccga 22980 gggccgcgct ggttggcaga taatatgaaa ccggcgcgtc cattggacgc tggcggcagc 23040 caatgggcgc gttgggtttt gtttacaagt tccctatata tattatatta taccttccct 23100 gttaagggaa tcccatgttc ttacatctaa tcagctgggt tacataatta gaatgtcagt 23160 aattactatt attactgtat tatttattaa attatttatt ttattattta tttaataaat 23220 taattcttgc gttattatgt aatcatttac tgagaaatct actaccaatt taataaaaat 23280 aaataattaa tacaattgtg gtgggggttc taaatattgt gcggaaaaac aatatttttt 23340 aaatctattc attaaaaatg cttctatttt aattgtgacg tgcgtattaa gaatgtggga 23400 gtggtttgta accatgtttt caaacaacac cattttgggc cgtctgaaac tcatataagc 23460 ggaaagctcg gcgttaattg ccactggccg ccaaccagtc caccttacca gttggagttt 23520 accactgctt acggctttac cttggcacag gctgatttac gtaacacgcg ttgggggttt 23580 aacccggttg aatttggttg tttgcacgtg caaaaaagcc caccgcggct tgggtttaag 23640 cgtttaaagc gttgctggtt ttatgacatg ctttttgatt taactgctat gggagctagc 23700 tcgtagcccg catgctttcg gtttagtggt tgtacaaaaa caatggctcg taaaccgcag 23760 cttttggatt gtcactggag ccaaaaacgg cgaacctacg caacctgccc cgcgtcgcgg 23820 tttctgtttc tagctcgctc gcactacatt ttaaatttta atttaaaatg gagcaatggc 23880 acggcgtaaa tttaagcaca agcacgttaa gcttttagat gaactaacgt aaccagtact 23940 tttggcgacc tggcgaattt aaaatttaat gccgtggtct ttaacacaaa gctgccagtt 24000 tgcaatacgc tgcatatata cagtgccgtt ctaattttat ggttaaaagg attttaaaat 24060 tgtgtgaatt ttgtaattgt gtacacgtga atttttaaat tgaatttaaa attgtaatta 24120 tgtacgcgtg aattttacca ttgtaattat gtattgaatt ttttaactgt gttatagttg 24180 tatttttgtt aatttgtgta attttgcttt tagatttgtt cgggtgtgaa ttccagacag 24240 gtaagatttt agctcctaat gtttgccttg ccgcctagct cctaatgttt gccttgccgc 24300 ctagctccta atgtttgcct tgccgcctag ctcctaatgt ttgccttgcc gcctagctcc 24360 taatgtttgc cttgccgcct agctcctaat gtttgccttg ccgcctagct cctaatgttt 24420 gccttgccgc ctagctccta atgtttgcct tgccgcctag ctcctaatgt ttgccttgcc 24480 gcctagctcc taatgtttgc ccacgtttat gtttaagcac actaaaattt aaaaacgttt 24540 gtgttggttt ttatgaccgg cttggtacaa aacctgctgg tgatttttta cccaacaaaa 24600 ataataaata aaaaagttaa aacttatttc tgttgtctgt ggtaattgcg ttccccgagg 24660 gtcccggtct ccccgttccc cgagggtccc ggtctccccg ttccccgagg gtcccggtct 24720 ccccgttccc cgagggtccc ggtctccccg ttccccgagg gtcccggtct ccccgttccc 24780 cgagggtccc ggtctccccg ttccccgagg gtcccggtct ccccgttccc cgagggtccc 24840 ggtctccccg ttccccgagg gtcccggtct ccccgttccc cgagggtccc ggtctccccg 24900 ttccccgagg gtcccggtct ccccgttccc cgagggtccc ggtctccccg ttccccgagg 24960 gtcccggtct ccccgttccc cgagggtccc ggtctccccg ttccccgagg gtcccggtct 25020 ccccgttccc cgagggtccc ggtctccccg ttccccgagg gtcccggtct ccccgttccc 25080 cgagggtccc ggtctccccg ttccccgctt taacgcaacg ttaaagtggt ttatttagca 25140 aacacgtttt tgctgcgtat ccatgcaaaa aataaaaagt tgggtttccg aagcgcatgg 25200 gtgctttagt gtttcatagc acgttttcgt gtcacagtag gagtggttag ttttttggta 25260 gcgtatgcaa ctaggtagct cgtctaaccg ggaaaggaaa cgttttaaac cgcagtgtta 25320 ccgcggtgtg gcatacggtt tacgtgcaac tgccggtacg cgcgtggtac ctgaggttac 25380 gtgtagcaat tatggcggct attcagggcc ctccgccgct ccctgaggag gaaaatgaaa 25440 attctttgcc agatgacgtg tatgctatag agggaatctt tctttactgt gggcttggac 25500 aggcggagta cttgcaccat cccgtgttta gccctatcaa ggaatttatc agctcctttc 25560 tcaaggacag cgcgcgcctt tacgaaaggc ttttgcgcca caccgattac cgctctttgc 25620 gcggactaaa cgccataggc caagggatgt tgcatataaa cacggacgga cgccacaact 25680 ggggtcgcgc tttggccgtg ttaggtcttg gcgcctatgt ggtggataaa attagagacg 25740 acgagcgtct tttaacgttc gctatagccg ttctacccgt gtacgcgtac gaggcgctgg 25800 agtctcagtg gtttcgttcg cacggcggat gggagggact ccggaattac tgcgagcgaa 25860 tactgaggca tcgccgcaat gcgaggagac acatgtgcta cggggtcgcg gctggtcttc 25920 tggcgctagt tgcgctgttt gccatcaggc gataggcgtg cgtttaaccg cgtatccccc 25980 taccctaacc ttaacttagc caattgtata taaaaccaat aaaacaaaac aagccaacgt 26040 gttattcgtt agaacatctt tttatttgag cagttcctcg cagaacattt tctgtatttg 26100 tgacacgggg gccggctgca cgctggcctc caccggggcc cgcgcggact gtccgcagtc 26160 tgaatcgagg ggcgggcacg cacccgcgcg gggggcagag gcggaaggaa cggcgtttga 26220 cattgccgat tcctgggcgg cgggggctgg agccaccggc tgcgtggcaa ggccggcgtg 26280 gtggctcgcc ggctgtgggg gcggcggctg cgtttgctgt atgccctgtg cgatctggta 26340 cggctgtgag gcgtggagat gggtgtccgt tcctggatac cactgcggct ggtacgctag 26400 gtacggcgca gacgcgtagg tttgcggcca cgagaactga acggggggtg gttgtggtcg 26460 ttggtcggtg tccttttctc cagaagtctg cgaagcggct cgtttcaggt ccctaagatc 26520 cgcctgaatg tccaatatgt ttttggacag cgccatgacg tccttgtgta tgccgacctc 26580 ctcgcctgga aacacgggct cgtcggaaag ttccacgtcc cgtttgcgct tctggtggcg 26640 agacggtgcc tgagcgtagc cgtacgtggg agaatagtac gtggcggcat acggagaggg 26700 ttggggggca aacgccgact gaaaagggaa cggtggcgct acgggcggcg cgtacgacgg 26760 gacggtcagt tctggtggcg gtatccacga gggatacgcc gccgttgccg gcatcgaggg 26820 tggcgcggaa acgtacgcgc gttggccctg gttgcgcatg tgatcgagac tgctctgcac 26880 catggttaga aaggtgctct tgggaatggt gatgttgtca tccgggaggg cgctcatggt 26940 ttgggtgtcg cggttaccgc cgtgctgaga ggagggagac tggctggcct ttaaatacgt 27000 acttctcgcg actctggcca cgcctttatc tgttttgagc aggtctgtgc gatctcggat 27060 aaatccggcg tcgatcgcct tggccatcag tgtttcaaga ggggctgcga attctggcgg 27120 tgtcacctga cgctcgcaaa gatctaaaca cttggacgtt attttaccgg cctcatctcg 27180 cgtaagagaa tcaaatttgg agacaaccca ggtagggtct ggtccgtaaa cggcgatgga 27240 ccccctacgc ctccccagtg cgcacagaga gacgtgctga aacgcgggtg ggtgattggg 27300 gtcttgcagc tcttctgggt gaagagacga gagggagagc tctgggagcc atgtgtgtaa 27360 catctccagc agggggtccc gaggcatggg gttaagctgg atttgggccg ctcgcgagtc 27420 ccccgcgagc cgtgacgcca gggccaaaaa atcggggctc gttagcttcc ccaggcaaaa 27480 tatcccgtgt gttacttgaa agagaccgag cgtgtgacct acgtgggctt ctgggacgtg 27540 ctctatgttt atcggtagag ggttcgtata cgggagcagg gtcgccacga ttgagggttc 27600 taaatacagg tccttttcta tctttggtag gctgaccacg tccacgtatc caccgacgta 27660 cacggaagtc atgttgggtc ggtgtttgcg tgagccgaag gagatgagcg ccggccttcg 27720 ggggctgatg tggcgcgtta tccgttgtga gaatttaaat acgtttctcc cgggcgagct 27780 caggtttctt cacctggtgc tgtgcgaaat gtacaactac ggtcttaatg tgtacctgct 27840 gaaggaggcg attgccaata ccggaacgag ggacgatatt gtcctcgggc gtaaggttcc 27900 ggtggagttc tggaaaatca tttacgatgg gttaagggag atgggggttt ctgacgcaac 27960 gttgctctca gaaaccaaaa ggggggcttt gtggctttac ttcaacgggc gtccgtgcct 28020 gttgaaaggt ttaggcgact acgttttttg tcgactgggg ttaagccaca gcgtacgcgt 28080 agtgccggaa aacctaacgg atgggaatta tctctataac ctgggcagcg ttataccatg 28140 tcgcctgcta gtggcgctga gctactgctt ggcgttttgg gggcacgccg accacgagcc 28200 ctgggtcagg ttgttcgccg gcaagatttt tatactgtac ttaataatat ccggccacat 28260 tatgccacga aagtcaatct tagaacaggt gggaacgtcc gggtacggtg gctttgtcga 28320 ggctgtgtgt cgcgacgttc gcgcggtcca cggcattccg gcgtgggatt ttgcggcagc 28380 ggctccggcg ttaacgtctc gacagacgga ctacctgttt gcgttcaata acagcgttgt 28440 gtagggtcgt ctcacactac cgacgtggcg accggcaggt atcccaggac caaaaaataa 28500 actttgtcgt agtcgtcgta aactccgaat tggctcttca ttatctcgtg tgttaaaccg 28560 gggggtgatg ggtgcgagag gatggcggcc aggccttcct cggccgttaa acgtagcgac 28620 gtttgggcct gaattaggct acccgcgtcc ctgaatgtaa gcttttggtt caggatgtca 28680 aaaatctcgt tgaatctgga gccggtcagg ttaacgaacg gacgagtgtg ttttaaatgg 28740 gaaatggcct ttgcctccag cgccgttaga tacgcaccag ggaacaaaaa cgacgtgggg 28800 gcgtcgggcg cgcgcgaaag aagcggggag atgtaatttt ctgtcaggaa atcaaaaagt 28860 tgtccctttt taaggtattg tttggacccc gacgggtctt ccaccttgga aaatctacca 28920 cccaggagcg aggccaggtt gaggcgccgg tggggcgatc tgggtgtgat ttgggccagt 28980 tccaataaca cgtaaaccaa aactagacag cccagcgccg ataggccggc gcgaaggttc 29040 cattggtacg cttgaaaggg aggcacgtcc tcgctaaaca aagtggtcgc aaggatgtat 29100 acgagatcgg ggccgggtgg ctgcccggta cctgggtttt tggaaccggg cagcagtccg 29160 ctctgtgcca acgtcgcgta tatcacgtgg tttgtaaaga agtccgcact gtactttgtt 29220 tctttgttta ggggcgctag agaggcgcgt tgcttcggat tcgaatatgt aaactcaaaa 29280 cccaggccct tcgtgttttg ttttaggtga gagataagcg tcgccagctt tgtgccgagg 29340 ttatcccaga ggccgtctcg agttggtggc aacggggtac ccgtccggtg acagtagtac 29400 ccgttgagga ggcacagcgc ggcctgcgtg tccgatacgt tgcggacatc cgcgtaaaag 29460 tcttgtgtaa tcgaggcggc tgttgagata acagcagaca ttagttttag ggacgtggag 29520 ttttgaaagt ttgtcgtgcc tcgcagatct ctggggaaca ccctgcgttg catggcgttg 29580 tcggtaaggc tactgtacca cggaccgtat tgtggcagcc attggttttg gttcatgtac 29640 aggctgggca ggagctccag acggagatcc tggtttaccg tgaagcccgg gtctccgggg 29700 gctatcgtga caacaaacgc gtctccatgt gtctgagggg cgattttggg tcgtgggttt 29760 attgacgttt gggtatcggc ggtttccctg gtcggggacc gcagatcccc gaccatgttt 29820 tgaattgtgt ctaggtcgcg catgaccatt tctgtttccc gttggtgcgt ctgcagcacg 29880 ttgtctagct ctagacggag caggtttttt cgcagcgtgt gaacccttag cgccagctgt 29940 tgatttcgca tcacaaacgc gtttcttctt tcttctatca gcgatggttt gtgaatgaac 30000 agaacgttgt ttggatgtgg ggcccagaaa gttgcggtaa tttgccgcgc tggttttcgt 30060 ggatatctca tacagcattt ttctgacgtg cgcatcttcc cattggctaa aaaacccgtt 30120 aagcgccacc gacgtggtgt tgataaatgt aggcggaaac gctgatgact cagtatgaat 30180 tgttttaagt gttttctggt tcttaaatag cagccagggc ctcaccgacc agttttcgtg 30240 ccctctcggc gcggctctgc ctatatatgc cacggaatct gtcagttggt gtaagccctg 30300 ccatcgctgt gatattttta ttgcgttacc gggaaatacg gccgcgctca ggcacgtttt 30360 gagttcaatc acgtagcacg ttttttgatg ttcgctatcg acggtcagca cacaatctgc 30420 tattcgcctg cccagggtaa cctcaaaaaa aatcctaaat ttaacgtctt tggttgcttc 30480 gcgtgttggg cggattgaaa gaaactttaa aatatcatca agcgaccggt gtttaattaa 30540 ccgtcggtat acggctaagt gggcgcgaat tccagcccgt ttgcgtgagg caggaagggc 30600 ttcgagggtc gcggcgtgtt tacattgatt cgcgaccgtc atggccgaag gagggtctgg 30660 ctttggcgac gagcttgtcc gtcagatgcg ggatcggaag cctagatggg acgaatcttc 30720 cgacgatacc gatgacgttg acaccgaaag caccgatctc gagtatgatg atgtgttccc 30780 cgtggttgat acgcacggct taacgagccc tggaagtcaa aactatgacg tacccacgtc 30840 tccgtccgga acgccgtggg aattactgca cccggacgct ctgtatgcgc agccgaggtg 30900 cccacctaaa agggcggccg tgccgggcgg tggtgcgcgg cccaaggtgt ccgcgttctc 30960 ggctagactt caatatgttg gacgacagag ttttggggat agagagacgc ggcagcttac 31020 cggggcccag ttttcttccg agagcgagca cgaatatgcg gaaataccgg agcgtactac 31080 acgcccggtt gaaagcgggg acaagagaca ttttacctct gggcgtaggg gtggaatttc 31140 gggaccctcg tcgtcaaaac ctagtaacgg tgcggggtta acacgtaaga ctaagacgtc 31200 gctgagtgtt agtcttaaaa acttgctgcg gataaaggac gatgatgtta aggttgatgt 31260 acccaggccg gttaccgtgc cggttcatct tatgcagccg catcctatga cggaatatag 31320 aaatgccttt ttaatctatc tagagggggt tatgggtgtt ggaaaaacaa cgctattgaa 31380 ttcaatgact ggcatggtgc cgcaggaaaa cgtcttaagc tgtccagagc ccatgaaatt 31440 ttggacgtgt gtttattcaa attgccttaa agagcagcgc agcatagtta agcaaggcac 31500 ccacgggaaa tcgatcactt ctgctcgcgt atacgcgtgt cagagcaagt ttgcgctacc 31560 ttttcgtgca acggccgccg gcatcggtcg caacctgcaa ccgtggctag tgggaaacgg 31620 tagcacaaag ccagcgaatt ggattgtttt tgacagacac ctactgtccg ccaccgttgt 31680 ttttccgctg gttcacgtaa agtacaacag gctaacgccg gatcatttgt ttcaaatcct 31740 atctcttttc tcggcacacg acggtgatgt ggtcgttttg ctaacgctca acagttcgga 31800 ggcgcacagg cgcattcaaa gtcgaggccg caaggaagaa aaaggaatca cgcaaaacta 31860 cttgcgacag gtagcgtggg cgtaccacgc cgtgttctgt acgtgggtga tgatgcaata 31920 tctcacaccg gaacaaatgg ttcagttgtg tgtacaaact gtgtccatag aggacatatg 31980 caatatgaat tccagattga ctcatcggtt tctaacccta acaaagttgc atgaacagag 32040 tatgatacca atggtggtag aaatgttagc agcggttaaa gaacacgtga ccttaatgga 32100 ggtctgtttg ggcctcttta aagagctacg aaagcttcag attttaattg ttgacgcggg 32160 agaacattta gatgatacgt gtggcctttg gggaaatatt tatgggcagg taatgtcaaa 32220 tgaggctatt aaaccacgag ccgtgaactg gccagccctt gaaagctaca ttcaaacgct 32280 aaccagcttg gaaagcaatg cagccaatta accacggttt gtgtttgttg gtaattacat 32340 tctctgtaat taatggatat gaatataatg aagaaaatgt acctggactt gaaatagttc 32400 tttttacccc tgccacaaca acaccagtta aaagcgatat atcaactgtg gaactggaat 32460 ttaacagaac acggtatcgt attaattgga aaaatgtaag tgaagtgtta acttctcgtg 32520 taatacaaga tgcttgggct agttcgaaaa ttctggaaac gttgcaagaa acgttacaaa 32580 aaagaaaagg tattttaaaa ttaaacatgg cttatgttag taataaagaa attaattttt 32640 gtaaaagttt ttctagttcc gaaataataa acattacctc agatttcaac tacagttcct 32700 tgcctggatt tcttggatcg tttgatgtta ttaatcatga attaacgcac ggagttttag 32760 tatcaaaacg tgaattattt acaaatgcct tggatataat gggacttttt tatgcaatca 32820 aattaaatgc agagacgttt aaaataacgt ttgatgaatc aaaagttatt atttcaggta 32880 ttatgacagc cgattggatt ttagtttcta ttgcaaattc aagttcagaa gttaatggtc 32940 agtgtgtggc gttgctattc ggtgatccgg aaaaatttcc accgctaaaa ggatatgttt 33000 catatcgtga tttagtggtc gtaagaaatg ataattatgc aatagcggta attgcaccta 33060 tgtctcatgg taccatggga ttaaactttt tgcctcaaaa tttaaccgac atattttttt 33120 ccattttgaa tagtccactt aaagtaataa attatttgaa aggcaaactt tttgaactgg 33180 aatcaaaagg agcatgccag aatccttcaa acgaacaaaa catattgtct ttattttttg 33240 aagtaactgc aattcacttt ttatatgtaa gaaatttaaa taaagaagaa ccagtaaacg 33300 ttggatgtgt tgtaaaacac gtggcagcct taaaaagttt ggaaaggttg tttaagttgt 33360 gcttcccggc atttgaatta cattcactta acttgtggac attgtcgcat cttgcagcat 33420 cacagatagc taatttaccg ccaaataatg taatgtcgtt aactatggat gaacaagaag 33480 ttgtattttc tatgttcaaa ctggcagata ataacaacgt aaatgaaatc attttaaacg 33540 aaattataaa cataagtgat caaatgtata ctatgtatag tgacatatat caactatcaa 33600 acacgtacag acaaacagtt atggatattt atgaagtgtt aacaacagta tccttaacta 33660 acgtaggtgc acgtgcagtc tatccataca tattgttcac atccatgtgt aataatgtag 33720 aaatatcata tatgattaat caaatatcaa aacccgatga cattactata tttcgcgtgt 33780 tttcgccttg ttttttaagt ttaaggtttg atttggatga aaacaagcta cggtccgacg 33840 caccgcaaac gtcaaagaga actggctcgg aactggcaca aggagcgtct ggtttttggc 33900 ggttgttgca tgcttttcac gccacgcgta taaacgagtt ttccgtcata aattgcacca 33960 gactggcgtg gaagcaagta accgcgctaa tgccgcttac gaacatcacg tacgtcataa 34020 gctccgtgcg cccggatcac gctcgcgttt acgaggtttc ggaggtgttc cttaacagcg 34080 cgatgtttgt ctcggccgtt tatccaaatt gttctcattt tacaccgccc ggtaccgccc 34140 tacacattcc gatattgtat aacttttccg ccccgaggat aggatgcccg ctgtgtgatt 34200 cgattgtttt gagctatgac gaaaaccagg gcttgcagac catgatgtac gtgtcaaacc 34260 cccaagttca agccaacctt ttttcccctt attcgccctt ttttgacaac gataattttc 34320 atatccatta tttgtggtta atgaacaacg gtaccgtcgt ggaaattcgg ggcttgtaca 34380 gaagacacgc actcagtgct attgcatttg tatttgcttt tattggaaca atgtctgctc 34440 tgtatttttt gttcaagctg ttttccatcc tggcctaaac tgttaataaa gcgtaaaact 34500 ttaaaaggtt gtttcccgtt tctttctgaa tagtcacgcg ggggttcaaa ttagcgagaa 34560 cctcaaatag aggcgtaccg tcacatattg attcaatcac ctctgcgcca acttgaatgg 34620 ccagatctcg attttgggga ggaaacatta gaaaatattt gtcggttgcg gttaataatt 34680 gctgaggagc ccgcgacgta actttaaaat ccttctgaaa gttgtgggac tctatggagt 34740 ttaaacaaaa caccatgtct tccaggcgct gttttacgcg cgaaagcata gattcgaagt 34800 attctctttg atacggggcc gccgccttac acgtattcgc gtatagcatt ttaaagtgaa 34860 acagaatatt ttccaaaccc aaacgctgca ataggacgtg ctttaaaaaa aggtgttgga 34920 taggctttag ttttaaatta ggtaagaaca ttatagagtt gttggcgcgt tgcatgattg 34980 tcacggtgtt aaatgcggta attggactct cgcctatttg tggctggcgc gaacccatgg 35040 caaaaaatat gtcggccagt aaacagtccg actgtacatc tgagtcgctg gtcgctggcg 35100 gctgcttgag aatggatcgt agttttttat cctccgatgt aaaaggcgcg ctacacaagg 35160 ttggtggcgc atttggatcg tattcttgcg tggtgtttgc cagttcgttt atggttatct 35220 gtttgttatt tgtaagagtt accggtgggg ttttgacggt cacatggacg gaaaatggcc 35280 tgtagtgcaa aaaaagagag ttactcgcga tcactaattt tgagtcttac ggtaattggc 35340 gtgtcatcga agtcagaact tctaattact gggtctctga acaatgatac gcctctctcg 35400 ccttcgtccg ttcccacgca caagcagctg tttagtgcgt agggatgggg tgacaccata 35460 attcgcaaca tcgataattc cggacgtttg ggggcataca atggcatcat gttagaatag 35520 atggtgccga attttttaaa cagcagggga aggggtacgg ccggtcccgg aagtccgacc 35580 atcgcggcca gtgccgacga gtacacgaca tgacagacgt actcgccgtt ggatagctgc 35640 actgcccccc cgactaagcg agctttcaaa tctggaattt ttatcattga ttttcctttg 35700 gtagttttag gaaccgcggc ggccctggct tcgtggttat atttttgctt tatgtctcca 35760 gtgaagtccc aggcgtctaa tagtgtgacg aattacctgt ggttttaagt ttgaaaacgc 35820 gtgaccggtc gttgctatga aagacataaa attggcgttg cgtcctaact cgtctaaccg 35880 tattttttta cttcgcacgt atatctttgg aatgaggttg cattttttat atcccagaat 35940 agcgcattcg tgtttgcttt tggtgtgact aatgatgcgt tttgaaaagt caaacgcgcc 36000 aaggcgggcg gctcggttca gggctcccag gtccaaacgc aaaaacgaac aacattccac 36060 caaacactca atgaaacgct tgtgcagagt ttgaatttgc gctttatttc tcgtctccag 36120 cgttgtgaat attgtgtttt tgacctggtc tattctagcg tatgggacgc tcaatattgg 36180 gtccaattca tccgaaagtt ttttaagtaa gggcctgccg tatattttag aaattgttgc 36240 agtggctgcc ttaaaccagg aaacattgca tccgtcttta ctagaaacca cggaagggaa 36300 attcgtggtc cagaaaacgt ctcgccgccc ccgtctaact atgtattggt tttcgagccc 36360 gtggaggtct aacgtagagt tccagttcgc aatcgaaacc gggaaaatgt gcttcaccgg 36420 caaaaagcac ctcaggtttc ccatagcgaa cataaagtgc agcatgtccc cgcttatgtt 36480 aacgttaatc gcagccccgt tgcacaggtt gtcggagtag aacacgctca cagtgaatga 36540 cggttctttc acggagaatt ttttcattac aaagttattt gtgagcctgg ggatgtcgat 36600 gattgactcg aaggtaccgg tgagagaccg gcacgtgatt ttggtattaa ttaccatatt 36660 ggtattgaaa actgagattt tgaagttgtg taaacttagg tgctttactg gatcgaacat 36720 gtctggaagc ggttcggtct ggtggtcgtg gtgcacttgt ttatgtcgat ctgggttttg 36780 attggcgtca aaaataaaat tgtgatctct atcttttgga gcgtattgaa ttcgcgaaaa 36840 catggcctct agaacgcgag gcgtttcgcc gggccccaaa aactcggtgt tgggatacag 36900 cctgtcgcac gaatgacaca cgtgttccgc gacagacatg cacattgcga cgcggaatat 36960 cggtacctct ggtggaaacg ttagatagta cgttgacttt ggcgtcacaa caactacctt 37020 gtacggtttt ttgccaggat cttttttgtt aattttcacc tgtagattta cgccaagcga 37080 ttgattgact atgttttggt agtcgatgat taattcgctc gccactctga tgtcctgaaa 37140 tttgttttgt tttgataggt tttttaaaag gaccgggttg gattcaatgt tgtaaataat 37200 taccgtttgg acgcgatgca gttcgggatg tgagatccaa tccgaagtga aacccaaaat 37260 gttaaatttt aagtaattca gatgcagttt tgcgcacggg ggcggacacc gagctagcgt 37320 gagggttttg aacggctcta aaagtttaaa gtaattctga taacacgtgc cgatcagatg 37380 ttccggcagt gtacgcgtga aggcggcaaa gcattcctcg aattcccata tttgaaggta 37440 acgacagaga attcgaaaca tgctttgata atttacgcca cataccatta atggcgaaca 37500 gtacagggac cgtaggattc gttcgtcgcg ttgaacccaa accgtgtcgg acagttcgta 37560 ggtgaagacg gtgggtaaaa acgtatgcgt ttcgatgtgg gaaaatgtac atccgatagc 37620 atcatcaatt attaaacccg gtcccgcgta ctcgttaccg gtcttgccaa cgataccacc 37680 ttggcggtgt ataaaagggt atagtccttc tcccaatacc agacgccgga gcgcacggca 37740 cgcgtaaaag gtggtctctg tttccatagc cctgtccaag acctctagcg agacgttttc 37800 aagaatctcg ttattggtgg ccaggcagca aaaaattgcc agttgagttt tgaaatcgga 37860 attggccggt gacggggtgt cagctgtcgc cgtagcggga cacgcgggca gaagaacagg 37920 gccctgcaac agcatcatgg aggcggctct ggaggtacga ccctttccat atatggccac 37980 ggaggccaac ctgcttcgtc aaatgaaaga gtcggcagcc agtggacttt ttaaaagttt 38040 tcaactgctg ttgggaaaag acgccaggga gggaggagtt caatttgagg gtcttttggg 38100 cgtgtatacc aacgtaattc agtttgtgaa gtttctggaa acgtcgctag cggttgcgtg 38160 cgttaacacc gagtttaagg acctcaaacg aatgacggat ggaaaaattc agtttaaggt 38220 atctgtgccg accattgcgt atggggacgg aaggcggccc acaaaacaaa aacaatacat 38280 tatcatgaag gcctgcaata agcatcacat cggtgccgag atagagctgt cgacggatga 38340 catagagctg ctattcattg acagagaaac cccgctcgat tacacagaat acgccggggc 38400 cgtaaaaacg attaccgcct ctctccagtt tggcgtggac gcgctggaga ggggcctggt 38460 agataccgta ttgaatgtta agcttaggtc cgccccgccg atgtttattc tgaaaacact 38520 atcagatccg gtctacaccg aacggggttt aaagaaggct gttaagtcag acatggtgtc 38580 catgttcaaa agctacctca tggacaactc gtttttcctt gacaaatcgg acatcgccgt 38640 taagggcaag cagtacgtgc tgtcggttct ctccgacatg gtgggggcgg tgtgtcacga 38700 aacggtcttt aaggggacga acacgtatct gtccgcctcg ggagagccga ttgccggagt 38760 catggagacc acggaaaatg taatgcgaaa actgttaaac atgctaggtc aggttgacgg 38820 tggcatgtcc ggtccggcgt cttacgccaa ttacgtcgtc aggggcgaaa atctcgtaac 38880 cgccgtaacg tacggtcgcg tcatgcggac gtttgaccag ttcatgaaac gcatcgtgga 38940 ccgtcccaac gcgcagccca acgttgacga tgatcgggac gcggtggcgg acgggcagga 39000 ctccctcgcc aaaacaccga tcgcggcggc tgttatccag atcggagata aactggtggc 39060 gttggaaagt ttacagcgaa tgtacaacga gacccagttt cccttcccgt taaacaggcg 39120 tatgcactat acttattttt tccccatcgg gttgcacatg ccacgtcctc agtattccac 39180 gtcggccacg attaaagggg tcgagaatcc agcggaacaa tccgtcgaaa cgtggattgt 39240 aaataaaaac aacgtcctgc tgagtttcaa ttatcaaaac gcgctaaagt ccatctgtca 39300 tcctcgcatg cacaacccga tcccgtgtgg gcaagctttg ggtcaggcgt ttcccgatcc 39360 tgggcacgtt cacaggtacg gtcaaaaatc tgagcacccc ccgaacatga acctatacgg 39420 gctggtgtac aactattacc agggcaaaaa cgtggcgcac gttccggata tcgccctgaa 39480 ggcgactatg accacggatg agttgctgca cccgacctcg cacgagacgc ttcgtttgga 39540 ggttcatccg atgtttgatt tttttgttca tcagcagcca ggtgcgcaag ccgcgtatag 39600 ggctacccac aggactatgg tgggtaacat tccgcaacca ctggcgccca acgagtttca 39660 aaacagcaga ggcctgcagt ttgacagagc ggcggccgtg gctcacgtgc tggaccagtc 39720 aaccatggaa attatccaag atacggcgtt tgacacgtca tacccactgc tttgttatgt 39780 cattgaatgc ctcgtccacg gacaggaaga caaattttta attaactctc ctttgattgc 39840 attaaccatt gaaacctact ggaacaacgc cggaaaactg gcgtttatta acagcttccc 39900 tatgctgcga tttatctgcg ttcacctggg caacggtagt atttctaagg acgtgtacgc 39960 ccattaccga aaagtttttg gcgagctcgt tgttttgcaa caggcgctct cgaaaattgc 40020 tggccacgag gtggtgggac gcaggccagc gtccgagctg attaactgtc ttcaggaccc 40080 caatcttttg ccgccctttg cttacaatga cgtttttacc aacctgctta ggcagtcctc 40140 gcggcaccct atggtactca taggagacga ggggtacgaa acggaaaatg acagggatac 40200 gtacattaac gtcagaggaa aaatggagga cctcgtcggt gacatggtta acatttacga 40260 aaccagaaac aacgcggatc atgacggccg ccacgtcctt gacgtcggtc cctttaacga 40320 aaacgaacag cacatggcgg tgctggaaaa gctcttttat tacgtggtcc tgccagcctg 40380 tgccaacggc cacgtctgcg gcatgggcgt cgattttgac aacgtggccc tggccctgac 40440 gtacaacggc ccggtgtttg cggacgtcgt gaaccccgac gatgagattt tggaccacct 40500 ggagaacggg acgctccgcg agatgctcga ggcctcggat atacacccca ccgttgacat 40560 gattcgaact ctttgcacgt cgtttctcac ctgcccgttt gtcacccagg cctcccgtgt 40620 cgtgacccag cgggaccccg cgcaactgtt aaccactcac gacgacggga gatacgtgag 40680 ccagactgtc ctcgttaacg ggttcgcggc gtttgctatt gcagataggt ctcgtgacgt 40740 cgccgagacc atgttttacc cggtgccgtt cacgaagctg tacagcgatc ccctggtggc 40800 ggccacgctg cacccgctgg tcgcaaatta cgtaacgcgg ctgccggccc agcgcgtgcc 40860 ggtcgcgttt aacgttcccc cggccctcat ggccgagtac gaggagtggc acaagtctcc 40920 tatattggcc tacgctaaca cctgcccgat tacgcctacg tcgttgagca ccctaacgag 40980 catgcacatg aagctgtccg cgccggggtt catctgccac gcaaagcaca aaattcaccc 41040 gggctttgcg atgaccgccg tccgaaccga tgaggtgttg gcggaaaact tgttattcag 41100 tgccagggcc tcgacgtcca tgtttttagg gcagccgtcg gttatgcgtc gggaagtcag 41160 ggcggacgca gtcacgtttg aggtgaatca cgagttggca tcactggaca tggcgctcgg 41220 ttattcttcc accatcacgc ccgcccacgt tgcggcgatt acctcggaca tgggcgttca 41280 ctgtcaggac ctgtttctca tgtttccagg ggactcgtac caggacagga ccctcaacga 41340 ctacgtcaaa caaaaagccg gatgccaacg attcggtggt ccgggccaga ttcgcgagcc 41400 cgtcgcttac gttgcggggg taccgcactc ggacaacata ccgggactca gccacggaca 41460 gctggccacg tgtgagattg ttttgacgcc agtcactgca gacgttacct attttcagac 41520 ccccaacagt ccccggggac gggcgtcctg cgtgatctcg tgtgacgcgt acaacaacga 41580 aagcgcggaa cgtttgctct ttgaccactc catcccggat tctgcctacg aataccgcac 41640 tacggttaac ccatgggcgt cgcagcaggg ctccctcgga gacgtgctgt acaactcaac 41700 ctcgcgccag gtcgcagtgc ccgggatgta cagtccgtgt cgccagtttt tccacaagga 41760 cgctattttg cgtaacaatc ggggcctgaa cacgctggtc acggagtacg cggcccgcct 41820 cacgggaacg cctgccacca gcgcgacgga cctgcagtac gtggtggtca acggaacgga 41880 tgtgtttttg gaacagccgt gccagtttct acaagaagcg tttcccacgc tcgccgccag 41940 tcacagggct ctgttggacg aatatatgtc gaataagctc acgcacgccc ctgtgcacat 42000 gggccattat atgattgagg aagtggcccc catgaaaaga ctattaaaga ttggaaacaa 42060 ggtcgcctat tagtttagct cagacggtct ggagctaact agagatggcc ctcgataaga 42120 gcatcgtggt ctcggtgacg tctagattat tcgctgacga gatagccaat cttcagtcaa 42180 aaataggatg cattttgcct ctcagagacg cccaccgtct gcagaatata caggcgctgg 42240 gtctggggaa cctgtgctcc agagattccg cggtggattt tattcaggca taccactatc 42300 tggacaaatg cacgctcgcc gtgttggaag aggtcggtcc caacagtttg cggctgacgc 42360 gcatcgatcc catggacaat taccaaataa aaaacgcgta ccaaccggcc ttccattggg 42420 ataactactc agaattggta gttataccac cggtctttgg gcgcaaagat gcgaccgtct 42480 cactggagtc taacgggttt gatgtggtct ttcctgccgt ggtgccagaa ccgctggcgc 42540 aaacagtgct tcaaaagctg ttgctgtata acatttacta ccgagtggcg gaaacgacgc 42600 ctaccgacgt taacctagcc gaggtgacgc tgtacacgac caatatcact tacatgggtc 42660 gtaactacgc cctggacatg gaccccgttg ggtcaagctc agctatgcgg atgctggatg 42720 acctatccat ttacctgtgc gtgttgtccg cgttgattcc acgtgggtgc gtaaggctac 42780 tgacctcatt ggtgcgccac aacaaacacg aattggttga gattttcgag ggggtggtgc 42840 cacctgaggt gcaggctctg gatctcaata acgtaagcgt ggccgacgac ataacgcgca 42900 tgggtgccct catgacctat ctacgaagtc tcagttctat atttaatctg ggccgcagac 42960 ttcacgttta cgcgttctca tcggacacga ataccgcttc ctgttggtgt gcatataact 43020 aaaaacgggc ctccctgtgc tttgacatgt caattcccaa aattatgacg gtgtcccggg 43080 acaacgaggg tacggtgtgt gaggtcgcgg tggacaacgg acggcacaga gcgatgattt 43140 attatcccaa gattacaaac tcgagcaacg agcgcgcggc acagcgcgcg gacgtcgtca 43200 aggaagcgtt tgataccgaa accccagtgg acatcgtaaa gcaaattgtg aacgagggtt 43260 tagctatatc caaaagaaat tgcgtccgtt tggcattgta cttatatttt tatctgcagt 43320 acgtgtgctt cgctatcctc atcacttggc aattaaaccc gcacatagac ccaccgggtc 43380 tggtgtttgc ggttaaccca atgggtccaa aacatgtgtc gaaactgccg catccggcta 43440 ttgttgcggt gggttgtggg acagacgcca tctgtaagaa ctgtagcgtc cccgatataa 43500 agactgagct tggagtggtc taccacaacg ggtctagcga ttctggtcag agcgcacact 43560 atgggctggc cctgttaaag gcggcctggc ttgttatggg aaatgtgtgt cccgagccag 43620 tagtgcggca aggcgctgaa ttacttggtc cgtggaaccg gacggcgtgg ttggatttta 43680 aatcggcgat ggcggcaacc acgttttgcg gatccagagg cgtcctctgg tcaccgattc 43740 atgaaaaaaa cctctgccgc cccacctgga atgatgtaat taacacatca tcctttttta 43800 caaatgaatc actctgtcca aatgtacctg gggtgtccga aattgtaata gtgcttaatg 43860 gtgatgcata agaacaataa acgtattccc acgcactcta tacgttgttt ttattggtct 43920 ggtgaggtat agacaggaat gggaggttcc gatggtgcct ataaagcaaa atggtcttag 43980 agtaacaata ttgcggatag aaaagtggtt tgtaaatatt ttcacccgaa caatatgact 44040 gcacacacga atggggttct aaccacgacg ggcgtttcca caagtcagcc ggaatcgttt 44100 caaatttctc cattttttcg cgtaattaca aaaccgccaa ttatgggctt gtttttctgc 44160 gtggctatgt gcattatcgc gttggtgtgg tacgtaatgc gtagggtgta ttgcaagggg 44220 cgcgttgttg ccgattcgtg tcgcgacccg cgtcgacccg cgtatgaaat gttgaatgtt 44280 agattgcgtc cgcacgggac caatccataa agaactttca ttgcgatagt taaaccgcac 44340 ggcgttctct cttgctcgtt tattctagcg atttaaaaac aaatttatcg ttagttgcca 44400 tgtagtgggc catgacggtg gcaacaagta cgtcgtccga catggttttt tgttttgcgc 44460 agtacgtgtg acctccgtct tttagtggaa tgcaacgtat tgccttgatt tgatctatta 44520 gatacgctac gggatcaaac gatagcttga tagtgtgaga caccacagtt tggctggcgc 44580 taaacgttcc cgagttcagt gcgtaaataa aagattcgaa cgccttggct ttctctggcc 44640 ccaacatgta aatgggcgaa cgtataagag tgtttttgtc cgcgtggtgt aaaaaactaa 44700 gagggaccga gcatatctcg tttaacacag tcgctatggc cactccggca tcttgactgc 44760 tgttgccttc cactgcgacg ttaacgtgca ggatctgagg atggagggta acaatcgctc 44820 gaatcaacgc agctgcacat gacgctatct ggtacgcggc agtgccggtt agatctctca 44880 ggaaaaaatg ttccacgcct aacaaaatgc atttaatcac cttgtgattt accgcgatca 44940 ccgcaccgat gccggtgccg gacgcgtcgg tgttgttggt gtatgccggg tctatgtaaa 45000 cgtggagaaa cggcttcatc gcgccctgta tatcttgtga cgtgctctct acgcggcaca 45060 gatccaactg tgacagcgaa gagtcgctga caatcttatg catactttgc gcggacgtgg 45120 cagcgtcccc cattagctcc gtggaaaatg cgccatccag aaaaagatta gttgtgctcc 45180 gtaccgtctc atcgatcgtt atataggccg ggatatgcag gcggtagcac gggcacgcca 45240 caaccgtgtc ttgcaagtta aaatcatctt tatgatccgg acatacgtag ctcaccacgt 45300 taagcatctt ttcgtgggcg tccttcaaat taagtaaaaa actagttgat ttgtcagatg 45360 agttactcga ggatataaaa atcagttttg cgtccttttg tagcatgaaa cccagaatcg 45420 cggggagggc atccttctta atgaagttcg cctcgtcgat atataggagg tggaacgtct 45480 gtcccctgat gctctagagg caaagggaaa cacaaaacta gttacgcggg catggagaac 45540 gaaacgccta aggatagaat ctcggaagct gactttcaac agtgtcagga attttttcac 45600 cgtcccatta gagaactaat ttcctctgga gctgaggccc tgaaccactt tagcctatcg 45660 gaagcagacg gacatagatt ggaacgaatt gtccttctcc tcgacctggt ggggacagaa 45720 tgtctttcct ataccacaat cgctgcaaag agtgtcaaat gacgcgcgtc aacagtccaa 45780 tatgtcaatt tcataacgta tctagcttat accagtgttt ggattgtaaa cgctatcacg 45840 tatgcgacgg gggacgagac tgcgtcattg tatacactcg cgagaatcta gtgtgtgatt 45900 taacgggaaa ctgcgttttg gataacgtgc aggacgtatg ttcgtacggt cctccagagc 45960 gccgcgcacc cgacgcattc atcgatcctc ttgtgtcgca cggcacgagg gagagtctca 46020 aaagcgatat attgaggtac ttcgagacgg taggtgtgaa atctgaggcg tattctaccg 46080 ttgtcaaaaa tggacaactg aatggcatca taggtagatt aatagacgct acgtttaatg 46140 agtgcctgcc ggtgatgagc gacggcgaag gcggcagaga tctcgcggcg agcatttaca 46200 tccacataat tatctccata tactccacta aaacggtgta tgataatctt ctatttaaat 46260 gtacgagaaa taaaaaatac gaccacattg taaaaaccat cagagcgcaa tggatgcgca 46320 tggtctcaac cggcgatccg tcgcgggtca atgcgacggg ttgtttcacg tgatacttcc 46380 gcgagggttt attctcgcta acaatattac gtgcggtgga cggcaacggt tttttgcgca 46440 cactcggttc gctgcatctg aacgcacgtc taaaacttta tacgtgtggg gacgggtatt 46500 tcaaaacacc gaccctggca gcggagacgg tccatccggg ccgtggtccg gactggcgat 46560 tagtctgcct ctgtttacca cgaatggaaa atttcatccg tttgatgtag ttatactcag 46620 ggccgagacg cctggctctg gaagctcgtg gaccgtgaag tttttgtata tgtcattaat 46680 tgcggcttac agaaacgcaa tgcgcggttt aaaagataaa gtttcacaat ccaccgatgc 46740 cgccgttgac ggtgaggttc atcctctgac cgtcttaaaa gaagcattgg tctcaccgga 46800 cacggctacg cgaccagtgt ccgcgtgcaa ccctctacag atgttgaccg gactcttaca 46860 gtctagggta cgggacgatt acgtgacaca ccaccgtgcg ctcgaacgcc cgggaaatgt 46920 gaggggacaa gtaagcgccc caacacgcac cgagatgccc aacggatcgc caagtcgtgt 46980 aaggcttgga ttccgccctc ccaaacaagc caactatcca aagacgtggg cgcaggcgcg 47040 gcacgttttc tcgtctcgca catattacgt gtgcgtctat gacaacgagg aattagatac 47100 caagtggcag cgacaagatc cgcggccgtt atctctagac tggtccgatc cggtcgcgta 47160 cctgttagaa ggagatttgt ttttaggagc caaacaaaat gcgtttgtgg attctctaga 47220 aaaaacgtgc aggtgtcaga actataccat taagcaattt tttccggttt cgataaatag 47280 ggacaacgac accgtcgatt taattaagga acattttata gaggcgtgct tggtgattag 47340 aaaccaggcg tcagagagga gtgcttgggt gaaggcggcg ctgtttcgca acgatagtaa 47400 cacgtattgg aaggatgttt tgggattatg ggagcatggg cctcataaac tgggtacggc 47460 tataaaacga ccaacatcag agccttgcaa tgccgacata gactggagtt ggctcctgtg 47520 tgacgcggat ataactaggt caattaacgg gcagtctacg gtctgcttag ttgtctcacc 47580 tgccctaatc gcctggctgg tgctcccggg gggctttgtt attaaaggcc gctacgacct 47640 atcaagtgag gatttaatgt tcgtggcttc gagatatggc cacccagcgg cgtgacattc 47700 ttaaatcgtt tttaaacaaa gaatgcatat ggttgcgaca cccgggtacg tccgcgtttg 47760 ttcgagttta caccgcgacc acggcgcatt ccgccgtctt tgacccgcca gtaactagcg 47820 aagatgcgat gtcacataac tgtttaaatg tcatgattat gctcatgaaa ccaaaggagt 47880 ttggaccgtg cgttaccgtg tacataaatg gagatattct agatttttgt gctacggaat 47940 atgtcgccat aagggaagtg cctggtaggg cggacctatg tttaattcgt tttggtaccc 48000 tttccaatgc gccgaggagc gttccgatac ccgggccatt aaacccacat ccgcgagaaa 48060 acgtgcccgg gctaacaaaa caggaaatta tatacacttc ccaaaccgtg cccagagcgc 48120 agatacaaga tgccatcaag gggaaagcgt tcaaacaaat aaatccgttt gtgtggtttg 48180 atggaggagc gttttggcaa ctgttcctct ctgtggatta tatgctgctc tgtcccgccc 48240 tcgagatagt tccgtctctg gccagaatcg ttggcctcct cacgcagtgc gataagagca 48300 cgtgtaagat atgcacgctg gcccacgtac acgttaacgc gtatcgcgga tacacgcctc 48360 ctgactcgca agggacctcc ccctcgtgcc cctgccttat ctcgtgcggg gccaggcacg 48420 cgacggatgt cctggttacc ggacacgtaa atctcttggg cctgctcttt gatccaaaag 48480 tactccccaa agtgtccaga ctgcgtttaa aaagaaaccc ccacccggtg ccgatagagg 48540 acgccatgtc tggcgttacg gccgaaggga ccgaggtgct acccacttcg caaccgtggg 48600 ccctcattcg cctgccggat ttagccagtc gtgtaatgct atacggctgc cagaatttaa 48660 aaacaatctg cttacgttct tattgaagca cgttgcacac atcagcgaac tcggtcgccg 48720 tcctgggctc gcgtacacga tggttccgtt ttccttcttt atgttcaggt tcttcgccgg 48780 aaaccacctg gatagcgtgg cgatgacctc ggagaaaacg gcattggcga cgtgtttttg 48840 gtgggccacg taccccacgt gaacgttttc aaccgacgaa agcagaacgc tgatgatggc 48900 aaccacgatc catgttttcc cgtggcgacg tgggataacg aagacgctgg ccttctgctt 48960 aaacgtctgt aacacgtcgt ccgtggtttc aaataaacca aagtgttgct taaacgtggc 49020 aaataactgg tgtgtctttt cgggtgcttt gatagacgcg ataaaataaa acgtgtgcat 49080 gattaactgt tgctgaaagg gctcgaggca acaaacccct ggcacgtaac tcccatttaa 49140 aaatgacgac aggttggcta aaaattgccg cagttctgca taaacaggac actctaggaa 49200 agcttcgtgg gtccgttggg ccgattggta ttccatgtgc tggtccttgg cgtctgccat 49260 tcggacccga caacatgtct gtctaaggta gttcgtgagc tcctcggtta accggggcaa 49320 cgtagcgtga ctagaaattc ggggcttccc caacgtaggg ggtggcatgg gttcttgaag 49380 tctgcggtag gtttgaagat aatcgtctaa aactgaacta tatgcattaa ctgcgtgaat 49440 aactcccaaa catgggtggg ccattcgttc ggttttgtcg ttgcccgata taataacggg 49500 cggttgacga aaccagtttt cgcacccacc gtccgtgacc gcgcgcaggt tattttgaag 49560 gcgttcgcga tagctggtta acaacatgtt cccttcgagt tttttgaata acgaaaaccc 49620 cgaaacggga cgtcgctttg tcaaaggcgt tcagttagct ttagacctgt gcgacaacac 49680 tcccggacag tttaaactag ttgaaacacc tcttaatagt tttctgctgg tatccaacgt 49740 tctgccggaa tcgcgcccgg ttagagactg tccgcaggcg gaagggtttg actttgaaca 49800 cattcacctc ccgaaactga cacgcatgca gcgtgtcctg gggagatact gcgaccatgt 49860 taacaacgac gacgatatgt gcgttaacgt aaaggccagg tcctcgaatg cacagggtgc 49920 cttgttttat ttgccgtatg gacaggacga gtggaattgg gcgctcacgt taaggaaaga 49980 caagttggtg aaaatggctg tagagggctt gtcagacccc acgacctgga aaggtttgga 50040 gcccgtggac cctttaccgc tcatatggct tctgttttac ggtccccggt cgttctgtcg 50100 ggaaccagaa tgcctatatg aacgtaattt tggtatgaag ggacccatac tcttaccgcc 50160 acatatgtat gccccccgaa aggacgtaat gacttttgtc catcacgtaa ttaagtacgt 50220 taaattctta tacgtgaacg ccggcggggg tctcgaaact gaactgtccc cgccgtttga 50280 ggcctcgcgg ttgcgctccg ccattgctcg tctcggggac gtggaagcgg atgacgcata 50340 cctgtccgca aagtgcatgt tgtgccacct gtacaagcaa aacgatacaa tttcgattca 50400 tgaaacacac gtgggcggag tcatcgcctt aggcggagac ggtgcgagat atataacgtc 50460 tagtgttcga actcaacggt gcacgagtcg gggagatttc gttttaatcc cgttgtacaa 50520 cattgaaggg ctcgtaagca tgataaggga acatggcctc agcaacagct aaaaaattgt 50580 taattaagtc cgagcttgag tcggagatca acaaaaaact gtccatctcc gtctttgaca 50640 ggtttggggc cgacagtgct gtgtttaacg cgcagtataa gggaaccagg gaatcgctgc 50700 ggtcgtacga cagcctgaaa aagaaggaca atctggcgac cgttgtcgga acgctagaaa 50760 cgtcgctgcg cgaaaaacaa agcgaattgg gattactaaa ggggtttaac agaaaaaaaa 50820 ttgaagagtt tgacgctgtg acggacgcgg ttcgcgacct caaggacgag ctgtacggag 50880 aactggagat tctaggtacg ctcaacgatg aatctgttcc cgtggaagaa gagtccccaa 50940 aggaccacat tattagatgg aaattggagc gtctgccaag agtgtgcccc aaaagccctt 51000 gatcccattc ccaaggttca gactgacctt gacagaaccg cactgtccca tataaccgtc 51060 attcgaaccc gcaagacgct cgcccaactt aagataccta acacctggag ccaatgtagt 51120 caccaggcga cggactggac cgccgtgctc ggacgcggct cgtatggtgt ggtgaggtcc 51180 atgtctctag gccgctgcgt taagcatttt ggcagccggc gtgagttttt ttacgagtgc 51240 atttttaacg atatcgtacg cgcccgccgg gagaaacatc ccctgaaccg cgggggtgac 51300 cgtatactgt gtttcctgga gccgtgcgta ccatgtcgcg ccctgatatt cccgcagtta 51360 accgggaatc tgctaaacgc ggattttaaa cacgtgaacc ctgaacggct ggccgttgaa 51420 ttctctgagc tgagggaagg cgttagcttt ctaaacaata tatgtggtat tgttcactgt 51480 gacatcagtc cagaaaatat acttataaaa ggggaactga caactgcgta ctggagactt 51540 atgatcggag atctagggtc cgcctcttta cacacgggaa ccccttggac cggagtgatg 51600 gtgacctcca aactcgggtt cgtgcagcac acgtatcatt ttaaggcacc ggccagattt 51660 atctgtaagc acatgtaccg gccgtcgtgt ctcctctacc ggtgtttgct gtcgtgcgcc 51720 gggggcccgc aggcgcgtat gctagatcag ccgttccaga tcactccaca actcggcctc 51780 acgattgaca tgtcgtccct gggttatagt ttgctagcat gcctagagaa atatcttcag 51840 ccagctgacc catttcccca gcagggagcg ttggcggacg cttcctccga atccgcccac 51900 ccattgttct atttgcgttg catggtgcca agagtagtca tcgccgaaat tttttctgtg 51960 gcctgggacg ttccactcga tttaggtatt gactcatctg gccacgcgcc agctattccc 52020 ttgagagaag cgtacaggcg gttttttgcc aaccagtgta gtttatatag ggcacaatac 52080 aaagaggatg cgttagaaaa cgcatcctcg cggctgtgca actcaaaact taaactagtt 52140 ctccaaaagc tgttggtcag ggactacttt agtcactgcg gaaactgcgg agatcatgga 52200 ttttttctca gatgagccta tggtacagga gatggcgctg cttgacattg atgaacagca 52260 gcgccatctt tcgaaaatga gcctggccaa ctttttaaaa catgagcgcg ttagggcgtt 52320 ttttaacgat aacaaaaaga aaataagcat gccggccata cggttcgtgt ataattttta 52380 tctgttcgcc aaggtgggag attttatcgg caacaccgaa gtgtacgatt tctacgttag 52440 ctgcgtgttt agggggaggc ggctaacgct cctgtcggac gtgtacgatg cgtgcctaaa 52500 catgcacccg cacgaccgac accacgtgtg tgcattgata gaacaggtaa cgcgcggcca 52560 aaacatcaat cctctatggg acgctttgag ggacggcata atttcgtctt caaaatttca 52620 ctgggccata aaacaacaga attcgtcaaa aaaaattttt aacccgtggc ctatagtcaa 52680 caatcacttt atcgcgggcc cgctcgcgtt tggactgcgt tgcgaggatg tggttaaaaa 52740 gatactggcg acgttgctgc atcccggcga ggcgcactgt gaaaactacg gatttatgca 52800 gagtccccat aacggcgtgt ttggggtctc cttggatttt ggaattaacg tcaagtctaa 52860 tccaaaagac ggcttggagt ttcacccaga ctgcaagatt tatgaaataa aatgccggtt 52920 caagtacacc ttttccaaga tggagtgtga cccaatttac gcagcgtatg ccaaacttta 52980 tcaaaagccc agcatgcaga cgcttaaggg gtttttgtac tcaatatcta aaccggcgat 53040 tgagtttgtc ggagaggaca agctccccag cgaagcggac tatctggtgg catatgacaa 53100 agaatgggag gtgtgtccgc ggaaaaagag gcgcttaact gcagtacacc atctagttaa 53160 aaagtgcatg attcacaact ctacggcgcc ttctgatgtg tatatattgt cagatccgca 53220 ggaaaccgga ggccaaatta atattaaagc tcatttaagc gccaacctat ttataaacgt 53280 caggcatccg tattattatc aagtgttgct gcaatccctt gttgtgcagg agtacatcag 53340 tctctccaag ggaactaaaa atttgggaac ccagaaaaac tttatagcga ctggattttt 53400 tagaaaaagg cagtttcaag acccgagcaa ctgcacgatc ggcgaatttg ccccgttgga 53460 tccacacgta gagataccga ccctgttaat cgtaacaccg gtgtattttc ccagcgtggc 53520 caaacaccaa ctggtaaagc aggccaccga attctgggcg gctagtgcta gtgaggcctt 53580 tcccgagcta ccatgggatt tatcctctct gtgtgccaac gccccaccaa cgccgtagat 53640 gtaaaggggg aacctataga tgtctccaaa gaattcgatc ctatcattgg agacgaaagc 53700 attgtcttgt taacggcaga tggaactgcc cccgcggcgc tgtacaaacc caaaaccaag 53760 ccgtccaaac ataaaaaaaa taaattatca gattttgttt aattatgcgt atctttattt 53820 gaatagggtg gatgggaggg aatagaggga atggaattaa gggaaggatg ggatgctaaa 53880 atcatatgta tttcggatat gcatcctcgt catcgctcac atcttcttct gtttcatata 53940 acgcgttcag ttccggggag tacttaactt ttgtcgtttt ctctttagag ccttgaggaa 54000 ggggtgcgta ttcgggcgcc tttgcgcacc atttccaatc gtttctgata attctcaaga 54060 taatggctag gatgcacgtg attggaatca tagagatgtt aacggctatg actttgtgca 54120 ggctggcaga tatgaatacc ttgtcgtatc gaacgactgg gagaagcaga atcaggtaac 54180 tgacaaaaac gccaacgtag aatccaatct ggtgctttag gtactttact agaaatagtt 54240 ctgtgttgat ataccaagct actgtaagga caaaaaacaa gtttattgaa ccaaaaacaa 54300 tatcggaaac gagcatatag aaactgtttc cgatggccat catcgttccg agggagaata 54360 ctaacatctc catggctatt aaggacagat aaagattggc gccaatcggt tttccgtaac 54420 gcagcagggt gtctagcaag ctattctcgg gaatctgctg ctctaaaacg cgtagagacc 54480 aggtggccga attgcacgat atcatagcct ggacgtgcgt aaacgatagg caaaaatgta 54540 tacagtatac aaacgaggcc aaaagtatat gtttgtacga caacacgtga ataaacaact 54600 gaatggtcca cagccgcaaa atagacataa aaactacgct gtgagaacct atgagcacga 54660 tccaggtctg gaggctggtc attgtcgtcg cgtgcacgcg cttggccttg aatatggcca 54720 ggatggccca cgcgtagtaa cacagcaaat atccgtccac caaaaacgcc cacgagatgt 54780 aaacaaacat ttctggtgct tccaaaaaca gcgtaggcgt caggtgttta gcagaacttc 54840 tgaccgttag gtttagtgcg ctgtagttaa ccagtgtgtt aaagtagcac ggaaatccaa 54900 gtcccgggaa tgtggcggtc agtggcacta ccgctgacat tataaacata agtccaagaa 54960 taaccagtag ttttacccat gacgataaga taaacgagtc gctccgtgaa attttcatag 55020 ttcagagaat ccgctcgctg gcgcgttcgg caaactagca gtaaaatcag caagtggctt 55080 acatgttacg gatttaaata ggctccgctt ttaaatatca cattctgtgc aaaggagtcg 55140 agccacggca ccatgaacgc ccgggaggtg gcactcacgg gacatgtttt gcacatatcg 55200 ctgcatagca cgcacgagcg cgagaaatta ataatctggc aggttcattt acttgtatgt 55260 caacaatgcg gaattcaagg agatgccgca tatctatttg tcaccgaaac attaagcaat 55320 actgactggg gaaatatacc ggcgataaac cgtcacgcac cgtctatgaa cgagcatggc 55380 cgtaattata tgcagtggga actccgtact cgtttacgga atcccatcat tcaatcgtta 55440 agccgccagc ccggtgcggt taacgtaagg gtcagcgagc caaacatggt gatagtgagc 55500 tgcgaacgag cgttgcatca ctcgtgttcg gtgcgcgtga ctggcgccta tcttcattgc 55560 aataccacta tggactttag gttggattct aacgtgtccc caacccggga attttggttc 55620 tcggagatgt tttctaaatg tttagtttcc aacatcgagg tctaccttaa aacaacgggc 55680 gggttatact atagggcatc gagtgccacg caatgccgga aaagggcgaa agatggcgca 55740 ttgggtattc tcgatatctt taattgcgaa tctcgtgaaa tacaagttgc cgggcagaag 55800 tacaacttga gtatcgccac cgcaaccttt cacgttcttt gggtggacga ggcgtgtatg 55860 tggaacgggg ccctggccga atttttcagg gcgctgcaca ataagttgtt tggcgaccgg 55920 gaaggcgtag cgccaacgtt aacgtacgtg tgtccggggg ccactccgga gggaaccccc 55980 ttccccccct acttttccgc gtttccacac ctcctgcttg tgtttggaag accgcgccgg 56040 ctcgacgtaa ccgcggtcca agaactccca aaagcacaaa tcgcggtaca ctggcccccg 56100 tttaaaaatt caatcttagg ggatcagctt ctcatacctg gcatttcacc taaaaagcca 56160 ggtaccgtac ccgttcgttg gccgctctgg gtgcaggatg ttaacttgag tctctgtgag 56220 acgaccgaaa gcgtcgcccg catagttgac ccacattcta tagtaatcat aaaaatttca 56280 acactgttgt gccagcacct aaaatgccac cgtgcgtttg tcaaaaacga gttagaatac 56340 atagcgacca tctgttccag cgaccttcgc cttttcatcc aagaggaata caaccggtta 56400 cttgccacaa tttttacgtg ggccgcggcg agtgggtata cctgggcggc cattgataaa 56460 acaacagtat tcatcaaagc tcctcagctc agcgcagctg taagtggttc ctgcccatca 56520 ctaaatagtt gccgtaggaa acaatattac aaaggtttaa aaataacagt tcatttcctt 56580 tcacaggaac agcaaaaggt cgtgacccgt cttgaggcgc agttgggact tcccgtacag 56640 gaaacttccc gcccacctga ctggctcaag tatgaggttt gctccgcgtc cgtgttttta 56700 aaaataccag ccggggtttt atatgccgga cttgcaaaag accccgttag tgaagcaaaa 56760 cgggactcgt ggctggactg tctggtagaa ggcgcgacgt tatcgcttaa caactcagtg 56820 ccaccaattg gggcgctggc gggtatctta cccacccttt ttgccaaaag gcggtgtgtt 56880 aatttttggc tcctgccacg cgagtgggta aaatcggcgc ctatatgccc tcccctaccg 56940 attgactgtg ttacgcctca acagtttgtc gtaaccaagc gtggaccgat ttgctggtat 57000 aaagaatggc cgttaccagt ggacgttgat tttatgtact acctacagga ggcactatgt 57060 gtttttagtg ttgtgtccaa cggggagggt acggagagtc acgcggacga tatacgacaa 57120 ttagagaagt ttgaaaaggt actatgttta ttttaaaaca aagtctgtct ggggaggctg 57180 tgtaggctgg ttatttgaaa atattttaat accgatgcgt tgtgaaggtg tctggtaaag 57240 atcgtgccgc aataaaatat attaaaagtc tccccgtggc tatcttcttc tacgttttct 57300 gtgagacgaa aggattccaa ataaatgggt tttagtaagc ctttcatgtc gtctgcgttt 57360 tcgtccaaca gcttatggag tttaaaccgc actaggggcg gaacgcgcaa aactccttgg 57420 ggtgggttta actcatggta tgccgccaag gtcgacgcta tcacttcgat cccatacaat 57480 ataaacgcgg aatcattaca cgtatacctc tcgtgtaggt acctggcccg gtcaagcgcg 57540 gacaggataa atgatagggg cggcttatcg tagttttcca gcatagacag aatgcagcag 57600 agttctgtta cgctcgcgct tgccggctta aacagctgca cgcggtcaga aaaaacgtgc 57660 ggatatatgt ccagtgtgtt gaccatgtcc tcgtgctcga ccacacacgc aaacacaaac 57720 ccggtaaacg ttgccgactg aagcctggtg cggacgtgca cgcctaaatc gggaacgttc 57780 agtcgtcctc gaacacacag cttaggcgta ttggaagcca tgcaaatgct gttttttttg 57840 tgtacttcca gcatcaggcg cggaagaact ggataattat agggccctct tgatgcgcat 57900 tctgtttcag gcattattgc ctccgatcgg tgctgctccc ccattaaacg cttcagtatt 57960 tggtccatcc gttccaggct ggataatttg ttcgcaatat ttgtggccta tgtcatttat 58020 atatacaaac agcctgctgt ccacatacag ctggtctgcg atatcgtgta aacttaagga 58080 aatgagcgag tgatttatta ggtccatgtg agtcaatttg gcgattatgt acgtaaacgg 58140 gcctaagaga atggaaacag tgtcttgcga gtaggcgatg ctcgttcgct gcccctgatt 58200 gtcgaccacg ggtgtgaggt tgtacgtttg aaacatttcc ccctcccaca ggctagttag 58260 ctctctgagc atctccataa acggaggaac gtattgtgaa aaaaagctgt ttaccacgga 58320 gctgccttta gggatgtgac attcggatag gttaatggtt gggtcgcgca aaccggatag 58380 agcctgcaac gtattctgag tgagtatatt aatatcgtgt ctgggcctgc ctccctctgg 58440 caaactctga agcaactgcg tttcgatgca ttgaatcttc tttacgtagt cgtctcgttc 58500 tttctcaagg ttagaaattg tatcgaactg ttcgttaatc tggttcgtca ggcacttgaa 58560 cacggtattt gaaacctgtt tccggagacc ctgggtcgta ctttccgtac cggtcccaaa 58620 gagcttgttt ttatccacga tgttctgaga gacgtctgtg acgaaatcct caacgacgtc 58680 tgttatgccg ctcactgttt tgttctccgc aagctttatc agcaagttta agagctccct 58740 cttggggtcg gttttttgag acgattgctc taagcgagcc agtatgtctt tatacatgtc 58800 gttgcacgtg ctgccgacca gcgcttttag aggcgcggta tttagtaact gacataactt 58860 tgcgtgttcc gcggtcctgt gacatgtcat aatcgcggta aataaccggt acagggggct 58920 atcaaaggag acgcgtccat tgtaaattat aggccgtgaa acaacctcaa ctgttatgtc 58980 tttttgtctg taggtgccga gataagcggc cttatctccg ttaaattcca cagacacctc 59040 agcgtagtct ggaatataaa tagacgtcac atcggtcatt atcgcggtaa tctcctgtgc 59100 cagtttgtct acgattcgcg atatcgtcac gtctccggaa gcgtgcgttt tcctcatctg 59160 ttgacagtgt gcttgtatcc tggcgatcgt ttcaccgtcg ggggcgcgcc tgacgattgg 59220 caccaacccc agggcgacca cccagtcgac gtatcgttcg tacgataaaa cagtcctggt 59280 gtgtagtacc tgattaatag tgttcagtaa cagttgatcg actgtcagac gaacggtacg 59340 ggcccacgat tcaaacgtgg accgtttaaa ttccggcgtc agatgctcca cgccgcgcca 59400 acgagtcttc agggtggtct cgaagttggt ccagtccttt aagacgttgt cgtatgtgca 59460 gctccccaat gccgtcttgt acaggtgtat aaacagctgt cttccaaaaa tccctggatt 59520 tcgaagactg gagtgtagcg tttgaccgcg aacgtacgcg tacttgccct gtaggatctc 59580 gaaaagcgag atggagagtt ccgtcggatg gaccaaacac gtcgaaccca gtccggggtt 59640 catcttgaac atgacgtccg atgccaaagt caggggtgtc gtggatcacg tcagtcgcct 59700 ctcaaatata actaccagcc caccggaaat gggttggtac gacctggcct ttgatccggc 59760 tgaagactcc gggccgttct tgccgtttac cgtttatcta attacgggaa cggctggcgc 59820 tgggaaaagt accagcatat cggccctgta ccaaaatttg aactgcctta tcacgggtgc 59880 gaccaccata gccgcacaga acctatcgcg tcgcctaaaa acgttctgtc ccacaatctt 59940 tagcgctttt ggctttaaga gccgacacat caatatcgcc gtcagaaaag cgcatcagac 60000 cggagcggta tccattgagc aagttcagca acaggagcta tcgaagtatt ggccggttat 60060 agtggacatc atgaaagagg ttatggcgaa aaaacccaac ggcatgtacg ggactatatc 60120 caacgcggat tttgaaaccc tctcgagaat gacaggaccg tgtttatgga cttccaatat 60180 tattgtgatt gacgaggccg gaaccctgtc ctcttacata cttaccaccg tcgtgttctt 60240 ttactggttc ctgaacagtt ggctaaatac ccctctttac cgccaggggg cggttccgtg 60300 tatagtatgt gtcggttcgc caacgcaaac caacgcgttc cagtcaactt acaaccacgg 60360 gacgcaaaag acggagatat cgtcgtgcga gaacatccta acattcatga tagggaaaaa 60420 agtcgtatct gagtacgtga acctggagag aaactgggcg ctgtttataa ataacaagcg 60480 ctgcaccgat ctgcagtttg gacacctttt aaaaattcta gagtacaatc ttcccattcc 60540 tgacgaagtc atgagttacg tagacaggtt tgtcgttcct aaaagtaaga ttatggatcc 60600 tttagaatac ataggctgga cccgactttt tttgtcacat agcgaggtaa aggcgtattt 60660 gacaaatcta cacacatgtc taacgctagg gggcgatacc agggacacga agctctttac 60720 ctgtcccgtg gtgtgcgagg tgttcgtgaa gccgtttgag gaatacaagc gggccgtcaa 60780 cctcacccac ctcaccgtaa ccgagtgggt gacaaaaaac ctctttaaat taagcaatta 60840 ttcgcagttt gtggaccagg acatgtccat agtcgccacg gaatccactg aacgttcgac 60900 ccaagttacc tttatcacta agtttgttaa aaacagccac gtgtctttaa atggaaaaac 60960 aaaaaaatgc atatgtgggt ttcagggtac gtactttgag ttcaagagaa tcctagacag 61020 cgaacttttt gtggagacac attcgcaaga ccgtccggaa tacgtatacg gcttcttaaa 61080 cacgctactg tacaacgcca tgtactcgtt tcacgcgtac ggcgtgacta gggcacacga 61140 gaaatatctg gaagatctga aatttgcacc actccccacc gctctggcga ccgggcgtgt 61200 agactttcaa acggtccgtg aagagttaaa cctggaagac gacatcttct accacgtgtg 61260 cagtccccca ccacccgcgg gtatcacctc tctccaggtc ttggtcgaca cgtactgcgc 61320 cctgaaggac gtgttcgcct ccaggataaa ggtggcgtgt cgctggtttg gcggggagtt 61380 tgagaaagaa acgttttccg cgtttacggt taacatggtc gtaagggacg gggttgactt 61440 tgtctcccct tcagaacgtc taaacgggtt gttggcgttt gcatcgaccg ttgaatcgta 61500 taaaattaag gggtacacgt ttttaccgat agcgttcggt cgctgccagg gattgccact 61560 cagtgatgac ctcaggaaga agatgccatc tctggtcgtg caggactcta gcggttttat 61620 cgcgtgccta gagaataaca tatccaaact gaccgaaacc atggatgatg ggagcgtttt 61680 tcaagtgtgt tgtgcggggg actatggggt tagctcaaat ttagccatga ccatcgtaaa 61740 ggcccagggg atgtcgttgg agcgagtagc cgtagtattc ggggcccaca aaaacgtcca 61800 aacaagccac gtgtatgtag caatatcaag ggctgtcaac tcaaattatc tggtgatgga 61860 cagcaacccc cttaaaaccc tcctcagaga accagtcgat aacacctccg ccaagcatat 61920 agtccgcgcc ctccacaacc caaacacaac cctaatctac taaataaaca aaaacaagca 61980 aatggaaaac actgtgtctt tattcagtcc agccacggcc acggatagtt gtcatttcca 62040 cacaccgggg gggtggccgc catagtttga cgaccagaaa cgcccggacc ctctgggtta 62100 gaagtagccc cgccccccgt ggtcgaggtc atacgtctct taggggcccg ggttgtaccc 62160 aaataaatca catcgtcgtc accgttgcag tccctgcgcg atgcgtgcct cttacaggcg 62220 gcacggacac cgccgcttgt aacgtgatct gcatcgtcgt cgctgtctga agacgaacac 62280 aggtcaatca catccgtggc gcccgtgccc tcatcggcgt ctgattcgtc ccatgtctca 62340 acagagccac ggtcgtccgt atcatcgtca tctgatataa taatggtctc ctgttctaca 62400 gctgatccag taacggcagg ttcttcttct tcattggacg accatccgcc ccctgccggt 62460 gatctagatg tatcacctga ccaggcaggc gaagcccgtg gcgaaaagcc atcagcatct 62520 tcgccactct catcagtgtc ctcatagtca tctataaaaa aatcgtctcc gctgtctgat 62580 gtagatgacg ggggtgcgcg gtgttggcca gtaaccaccg cgacgggccg ttgaccacca 62640 aaagcggtca gtggcgcagg cgcgcttggt tgtgcggcgg gacctgccgc cgtaatgacg 62700 gtaggtcgcc agtcgctctg gttaaaggac tcaccgtccc gtgcgtgcgg atctatccta 62760 ggtggggagg agaccggttg ttcgtcttct tcatccatgt cactgtagtt gctgttctcc 62820 gaatgagagt cggtttcgtc tggcgttttt ggagtggtgg gaggagaatc tgcatcaaaa 62880 acatcgttag gtgcagtcat gtcaatcaca ggggggcctc cgtaaccggg cggtaccggc 62940 aaccccgtac gggacccggc gaacagaaac cgtcttgttc tctttttcct aggtgcaccg 63000 ggaatcggca acatcctggg agtggccggc ggggtccttg gagggtccga caagaacata 63060 gccatgacca aaacgttcac ctgtaaaacg cgccgcctat ccccgatcag ttaatattcc 63120 aatcaacggc gcccctctga ttttgaacta gatagtcatt cgcaagttta aaatggttgc 63180 agcctagaaa ctgcggccag ggagaaccgg tggccgcgtg agcggcagct aggggagacg 63240 gatggcgtgc cttgaggacg agatgtctct ggccgtttat caacaccgcc ttgtctatgg 63300 cttttcttcc ccacagcata aaaacgcacc gctgaagctt ggcagaaagg cagcttatta 63360 tgtagctggt gaaccaatcc cagccaaggt tggagtgtga ccccgccttc cctctctcca 63420 ccgtcaggat ggtgtttaaa agcagaactc cccgtttcgc ccaacagtct aagcacccgt 63480 gagaaggagc ggtgaaccca ggtacagtgt tggctatttc tttaaaaata tttttgaggc 63540 ttggaggtat actgtagtcc ggagcaacgc taaaggcgag tccggtggct tgaccgcgat 63600 ggtaaggatc ctggccaaga atcacgactt taatatcctc cggttcgcaa caatacgacc 63660 accacataat tctgtctata ggtggataaa tcacggttgc tttgctcata tccataacgc 63720 gcctcaacag agccgcaagc ttctttttta aaaatggaga aagatttaaa aatttaagcc 63780 atgagtcact aataagtaac atttgcgtgg gtgtttcatt tggtcctgtc atggacattt 63840 tgtgccaaac tactgtctcg agccaagtat ccataggtcc ccacgcctgg cacctacttt 63900 acgtgtgcga aaagctgcac tacctttttt cgttaagtcc ggcaccgctg gtaaattagt 63960 tacactttcg ctattatcat gcgtgtcctt aaaggcagac aaaaaatctt ccaaactaat 64020 gcgaacgtaa ttcagcaagt caagttcctc tcgatgaacg ctaaaatcaa gcccacttaa 64080 aattcttata aaaaatgccc taaggtgaaa accattcaca cataactctg tagtaattgt 64140 tccaacttta tatcgcaagg ttgcaacgca ccgtccttgg caccatgcca aatctgtaaa 64200 gtggaaagaa acaatttcaa atggtgcagg aatattaact ccagttagcg gcacaatgtc 64260 acaacatgga tttggaatta aaccactaga gtagccaata tatagtatga aataagttgt 64320 aaaaaaactt aatgtataca tatttcttgt atttcttact taatgtaaat gtgaacttcg 64380 tacttatata tacattgtaa actgcatgta tattgtatag gttaatagat ttaaaaagaa 64440 agtacctaaa aatacgtact ttcggatatc cgcccagctg ttaacccgaa aatacagaaa 64500 tgactacaca aacacacatg aaaccaattt tattcttaac acatgcaaca atatttcaat 64560 gtaacaccat gttaataaaa atacgcagca tgcacatttt tagctaagct cctcaaatac 64620 aatttcctct tcaattgttg actcatcaac ctcggtttcc gtgtcaatgt cggaaatatg 64680 tgagtccagg ataccctcat catcgtcaca aattaattcc agggcttgta aaatatcatc 64740 cagtgaatca gctgctagtg tcaaggatgt tgtttctaat tttagcccat caaaacggtg 64800 agtgggtgac attttgggac aagaccccgt gaaattggca cgctcaacac aaacggaagg 64860 atacatttga ttattcacga ggggcagcat atttattttt ataacatcag gaaccggacc 64920 cgccaatgac gcacatatgt ccattaaaat cggagtcgtg acacgggttg aattgacggt 64980 gaaaaaaaat gtattagctg cacatgcgca actatttttt aaccacacga gggcggaata 65040 aaacgggtcc cgggtgctaa ggccgcggat tcggcaggca cggctcattg ccatctctag 65100 atttgttaaa tctgttcgaa tatacgagtc taaaattaag tataaccacg acaagttcat 65160 gcaggaggca acgcggctgg tttccacccg gacatccccg ctcacaaacc cgaactctct 65220 aggaacgcac atcaaagcgt tcaggcaaaa ttccgaaacc gaaaccctag ttctgagcac 65280 catctggtta taaactgcgg ttaagaggcg agcggcccca cactgctgct tgtgaggatt 65340 caacttaggt ggcctgcagg cttgctgaca gtcccgtagc tgcctggcgg cgctcgtgca 65400 gctctgacag ccgcacgcca gttccaaagc gaggcagaag cgctctttgc agtcgcgcca 65460 tatctcggtc acaggagatt cgctcgcatg atcttttaag tgcatatata tctgttgggt 65520 aacaaacctc actccctgta aaaggggaat aatgtccgtt ctttctatcg tcttctctga 65580 gtctatagct acatctttaa gtataaccaa agacgctaaa aacccaggat ggtcgacccc 65640 tttaaaaaat cgcaaaagcg accggatggc tctatccgcg tttccatgtt gttcaaaggt 65700 agtcacgatg gatctccagt tagactcggt ctccctgtca acaccctgaa ctggaatgga 65760 aacagccatg acaccgtgaa cttcctgatg tctcctaaaa ctaaccccga aacagagcta 65820 aataccaatg actgtcaccc ctaccccaag ccacgccccc gtactattag accagggtga 65880 gtaaccacgc tatcctttaa aaacccatac gtggagtttg taaggtaaac agctcgtgta 65940 tatttcagac gcctgtcata aaatggatac cgacgacaat caggtaatta aacttttttt 66000 tattcaagat tcaggagggc gtgtttacag tggtgtaggt gggagcatat ctcgccgatg 66060 ggaatggctg atgaatccac acttagtgct cggatcaggt gctctgtgta ttttactagt 66120 gcagctgaac ctaaatttgg cgtgtttagg tcgtaccaac caaaaaactg cctggcctcg 66180 ccttttagga gctctatgca agctttaatg gtgtccaata gcttgtcttt aaaaatgcaa 66240 ctctggtaca tctttatgac agtggtccaa aaaaaacaaa gatttaaaaa cacgttaaac 66300 tgcgtgtcct ggtagtcctc gtatatcacc tcctcaacaa gaaaaaattt tttaaccaaa 66360 ctcgccaggt actgaaacga tggtacggac aggtcgtgga aagtgtctat catttccttc 66420 acctcccctt taaaggtttt ggttacaccg accatgtgag ataggcacca gctcaggggc 66480 gaggtcggat cgtgaggggg caacaattcg tggacgtggg ggtactccag ttttaggatc 66540 tccggcagga tgcgtacgag ttcttcgtca aatcctacgc agcccgcatc caccaggggc 66600 agtactgagt tgataagtcc ccgaattcta tcgttcgtaa ttttgtggag ctcctttaga 66660 cagtaaacca tgttgctccg gcactgcggc acaatgaacc gctctccttg tctgtgctgc 66720 ataagcacct ggagtatctt agacaggtat agcgcccgtt ccactctcag ggttgccgct 66780 tggtagagcg gattgcgggc attgacggtc agtgtgttca tctcaccgac tatcatgcca 66840 agcggcggat agtggaactt atacatatga tttaaaagat ggtctttccc gtaatggcga 66900 ctcatggccg tgttttaacg ttcacagggt gttaaaaaac tcagaaggtc ctgcgtggac 66960 aacttttgcg gactctccga accgctcagg gataagctgt accacgcggt gcttcttata 67020 aacgaagcat acgtcaagaa acatgaccca cgtgacctaa ataagctcac agaagaagtc 67080 tgtcgatgta ttgtaatgga atgtgcctcc ctgggtccca tctccgggct cattgcggat 67140 ttgaatctct ttaacctgtt ctgcctttac cggggttccc gggttaaaac ccgcggagcc 67200 gccacgtgta acgtcccgtg cgcagaatgc gcacagggcg tcgtgagaat cctgaccgag 67260 agggctctct gttgtaccga aaagatgttc atagcgtctg cctgtagcgg ggttgtttta 67320 ccgccccagc tggccaaagt tttccacgac gtctacgcgg agatgaaggc caagtgttta 67380 ggggcgtggc gtcgtctcat atgttgcagg agacctatca tggctattgc cgactcggtt 67440 ctcgtcactt ataataccct ggatgccgag ggaaaactgg accttaaact caaagcactg 67500 tgcaaacttg tttttcaacc catctttctt caaagaatct tagcccctat gcagctactg 67560 gccaacggga aaatggtccc cgacaattat tttaccatta ccggcacggc cgagaagagg 67620 cgccctgtcg tgactggaag tactagcggg atgacgtgtc cgggaagcag ccttgtcccc 67680 gattccttaa tcctgccagt atgcgaaccg gggcttctcc cggcacccct ggttgacctc 67740 agtaatgtct tagaaaatcc agaaatcatc ctcagcgccc cacccctgag tcaatttgtc 67800 atcaccaaca cgcaccccag tctgcctcag tcagtcagca ttattacgcc aactcagggc 67860 gttgttcctg gccaatgttt tatggacacg tggaaagcgg tgtcacagag cattcaccat 67920 caggcacata cgcctatttt tgccgccacg ctggccggtt caacatccgc ggcccccggc 67980 ccgcatatcg catgttcccc agttgccggc acgtctcggc aggtggaagc gtccgcgggc 68040 gttgactgcg ggaaacccgt atgcgcgccg cagcccgata taccgcccca tgtccccacc 68100 aaaaggatgg aaacggtagc acagtcggga aacgctcccg taaaaaacgt ccacatcgga 68160 ggccgcgtat acgcgccact ggttaatata ccaataatag acttaacgtc cccgtccggc 68220 tccggacaga gtccggtcaa tatcgccaac actccagagt cccgcatggc ggccggctct 68280 ccgccctttg ccgaaacggc cgcaacggtc cccgctaaga gaaagcagcc acgcgaggac 68340 gtggcagaca aaagatcgaa gggcgacggt cggggcgccg caacagtaaa ccccccattc 68400 ccgggaccgc ccgcgatgcg cgttcgcgag cagggcttat tcgatttaat cgaaagctcc 68460 acggatgtaa ccgcgaacgc atcggggcca aaaaatgacg acgacatgtt agcggctatc 68520 ctacaggacc tatatggcct acaatccccc cctgctattg attccccctc cagcaactcg 68580 gataatgagg acatatttcc agaggtcagt ccgccatcta gcggtcacgg atcgccttga 68640 aggatgaccc caagacacaa gatcacatta ccgacacctt cccacgcaac ccggcggatg 68700 tctagccgta aaaaatatca ccggttggaa agtccctggt gcgacaaaca taagcttcaa 68760 acttacccat tttctgtgct atttcgggac actaaaaaat tgtcgccact ggcgacaatt 68820 ttttagtgtg tctaagtgtc actcattttc aagtttctgt cctagaattt tcacatccag 68880 tttcatatca tataaagaca tctgttttgc tttcgtgaac ctggcgtgtt tttattttga 68940 aaggcgccct aaaaacatgc ctcgtgtgaa aacacaaccc aagagacccc aagtgtttga 69000 ctttatgcca ctagatctcc acggtgaaac acgcgcggag atggattctc aaagcctgtg 69060 tcctgacggt caggatctgc ttgggtctta tatctatacg gagaataacg gcccgttttc 69120 ccagatgatg cacaatggac agagcaataa cgggacaggt gaaagcttcg gcagctatgc 69180 tgccggcgac ggttttctgg gcggttctgt gtcagggatg catggaaacg gcaccgtaga 69240 tggcttgtgt tctaaaaaac aatccgcgtg ccgtaaacgc tcggctgcac taatccacgc 69300 agcgtccgaa gcgtctgtgg ccgagcaagg cacctcacag gggacaaatg ccgtatctga 69360 ccggataggc agagacggtg gcattggcaa taaactactc aaggtgagtg cgcggctgcc 69420 tgataaaaca aaaacgcttc cggatccatc cttgcactgc tatttttgat gtttaacacg 69480 taatgtctgt ttatgttaac cccgccatag cccgaaccca acattgtgcc atccgattat 69540 aaaacgcaac actcggacac ggcagatgga cgcacaaaac gcgcgcggca gtgcaagacg 69600 tcaggaaaaa ataaagtcca acagctgcag caggtacaat aagcaaattt agtaatctgt 69660 attttttaag tctccgaggt tttcccgctg gcatgcggca ccgtgtccgt gctttagttg 69720 caataccttc tcttaacaag cacgtattcc aacaggagct ggaaagtaaa acaactcaac 69780 tcaccgtcct caccgctcaa cacgaagccc ttcaaaagca cgcatcattt ttacagaaga 69840 tgatgatatt gatgtgcaaa aacgggaaca gcagtaaaaa aagcacgtca tgatttaaag 69900 ccaccccggg tcattagttt aaaactgcct aattgattct attcaccctt caataaaata 69960 aaattttaat acgtttgtgg tttgcccatt tcctgtctta aaaatattaa acaattcatt 70020 tgggaatgag gatttatggg attaagggat taaatttttt tgggatcatg ggattttgga 70080 acatacctct gggatggggg ttatgcttca tggtctgggt ggcgtggatt gcacggggac 70140 ggtcggtgtg cccaacctgg cacctgacgg atgggaaata cgaggcggta tacaggcact 70200 acctcgaaga gtgtcgcaaa catgaaggct cggggagccc ggacggttcc ggaaagaccg 70260 aggggtctgg aaccaaagca accaccgaag cgaatatatc gatacgacct aacgttgtta 70320 cgtcaggtca agataaagag ccgatgaaga cagcaccgag ggccgaatca tcacacgacc 70380 tgccacgcat cgagcaggtt aacgctctcc acttatcaac cccggaattg gcgcaacccc 70440 tcccggtagt agaatcgact ccacgcgagt cacagtcagg tgggacaccc tgggacgcgc 70500 gcccccacgc gttcattatg cacacaaacg acatgctcaa cccatctgtg gtcctgtctt 70560 tcagagccgt ccgtgcgcgc tccatacgcg ataccgagca gtccattcgc gatcggaaca 70620 cggtcacgac cagctatcgt acccctggcc gcccttccct cgttcaagcc agaccctcgt 70680 cttacggtgc gcgtctaccc ccttcgcccc gaacaatggc aagatacgcc gagacgcgac 70740 caacagacga ccaaaactga acacaaagaa gaccgcgctg tccattcgac gcagtgcccg 70800 cacgggcgct gcgcgggacc tcgggcgtac gtgtcagacc cgcgcctccc tccgacaacg 70860 caatggcacc tggttaaccc cctgtgggcc atggccggaa tattgggcct cacgatcgcc 70920 tggtacacaa tatatcaaat atatgcacat agaaactaca cgacgcttca ctgcgaataa 70980 aggtttattt atttcacacg ctaatcagcg tcgttatttc tggtcctgga ctgggcgcgc 71040 cgcctcctga gcgccccgtc cgcactggcc gtgattccgc ctctggtggt ctcgtccatc 71100 gacacgtcca cgcggatgtt aattccggcg agggcttctt ccacctgccc gcgcgtcacg 71160 gccttggccg tgaccgccct caccttagct tcaattttac gggttgccac gttacataag 71220 gccgaaacgg cggccgcgat tttggcctcc ttttcgctgt tagagatgac ggggtcggag 71280 ccggacctgg tgggatcccc agaattaatc agctttttga gctgcttgtt ttcaacggac 71340 aatttttgca cctgagcggc taactcctcc atcgttagct cttttttggg ggcgcgcgtc 71400 ttgggacgcg tggaagacat ggccgctact acgcattaca gactacagcg gtacgtttaa 71460 atacttttag gcggccctga ggttactcgt gcgccacagt ttcaacaaat ttaaagaagc 71520 acatatatgt caggtacaga aatgttgcaa ccgcaaccag aacagagttg atcaccgccc 71580 atatgctcga aaaactagac agcacgggct ggtacgtgtc cgccgagcaa tcatagtcat 71640 aaaaagaggg cgttacggag ggagccgcgg agggggttgt agtcacagga ggcgtgcccg 71700 ttccggtagt cgaggaggtg gtgactgtgg cgcacaccgg cagacacaga tataagcacg 71760 ccgtcagggc taacgcgagc acaattgacc ccgtcatttt aaagccggcg ttcggcagac 71820 aaccctccac tttggcacac gagctctcct tatatactat cagttaaaca ttatggcaga 71880 agtaaccgcc catacggtcg catacgcctt tgactcctgt aagtttgaaa taataccaaa 71940 aaacaactca tctcgtatag cgttacgcaa caaatttcca gtcgtggtaa aaccgggaga 72000 accgctggtc gtgcccctgg ggctaagaat tatccgcgcg ccacagtgcg catttttcct 72060 cagcggagcg ccgacggatg aggtgtatta ccacaccgga cttatagatc aagggtatcg 72120 cggagaaata aaactcatcg ttctcaataa gactaaacag agcgtcacac tttaccgggg 72180 agaagtcaac gtctcactca tcgcgtttat gtacgcctcg cccgggcccc taaaatgtcc 72240 gatactgaac ctaccacatt actctctgga cgctggattt gatgtcacgt cgccacatgc 72300 catgaccatc cccccgactg accgaacccc gtttacgttg agtttgtatt ataagagtcc 72360 gcagctcagc accccccacg tcccactaat cgtggggcgc tctggactgg cggcaaaggg 72420 gctgaccgtc gacgcgacca aatggaccca atcgttggtc catttgaggt tctataactt 72480 caccaaagag ccaatagata tacccgcaaa cagccgcata tgtcaggtag tgtttattca 72540 cgaagaccac gtcccaagcg ggtggaacat tctgagatcc cgcgtacaac tcggcagcac 72600 cctccagata tcgtgggcca aaatcaggtt caccgacgtg gccacgcttc ccgcaaccca 72660 cccgctcaac tcccgcccca ctcaaagcca gaccgaacca gagaccaacc gcggcgcaaa 72720 ggggttgggg tcgtcagggt tataatttta aaacatggta ttattttaaa gttgtttatt 72780 tttaataaaa caatccaaat taacattaac catcagcctg ggcatcttgt attattttgt 72840 ctggcacgat attatccgcc accgccaact ggggcgtcgg ttgtcgaatc accggatggg 72900 aggggttgga ggacgcttcg gtatctacca gcacattatt aatttccgca gcccacgtga 72960 cagagtcatc ggacgcaatt gtcgtagcca gcttttccat ttccaggagt gacacggtct 73020 cgtcggcccg tttattcaaa agcgcgtgaa aggcgctctc gtccaccgta atatccccta 73080 tagccaggga caacatggcg ttccagataa cgttctgtat agactttagc ttagatattt 73140 gaatcctaac cgtctcctgg caccccgcgg gtaccctggc cgcgtcaaaa cgacgaagat 73200 actcggtaat tttattggat tgaacggcca acagataggt ctgtcggagg gcggcggtgc 73260 acatctctgc ctgcttcaca tcgcccatat ccactcccgg gggcagaccc atggctatct 73320 cggtccgcca gtgagtagga cactcgttaa gaggatctgg cagcggacga taccgacatc 73380 ccacgcgtcc aaacggacta aacccgcaac acgtccaaaa tgagccaggt gcggccattg 73440 ccagacgaac gggtaaatga aattagggca attttctcca ctagtggaga tatggccgaa 73500 gtaattacgg atatactaac tggaacgcaa gcaacggcgt ccttcttctg cgtgcttcac 73560 gatcggggca acgtgcctat aaatactcca cacgccgtga ttaaactctg cctgcccgcc 73620 agacgcccag gcggcgggcc aaggtgttta ccattgatgg tgctgaatct accggcgtgg 73680 caggttcatc tattcctaac aggtgacgca ccattgacct cggataacat taaagaccgc 73740 attgatctgg cccagaccga ggagatactc gagcccatat taagcgtact ggcatgcaaa 73800 cggtcggcgc agcagaccaa acatgactcg tttaaatcta aggtggcctg gtttagggca 73860 aagttcgtct cggccctaag aaaagtttac aaaatgaccc catccccata ttggatgata 73920 acgctgttgg gctcgttcga ggcatcgttt gtgctagccg gcacgtttta ttttttccag 73980 tcttatacct gtacggcgga gacgctggtg catctgacaa gactattcat ttccagccag 74040 ggccaaagct tggtcaccgt aaacacctat gacgaattgg ggcgtgtatt cgggcggtca 74100 gattttcttg aaattgttcc aaatttttgg gcatatctca aatacaagat gcagcaggac 74160 gacgtggagt ccaaggccat tgatcaaaca atcaactcca tacgtggggg gttgatgctg 74220 tcacctcagg acctcgtaca cttcatctac ctgtcatttt acgagtgcat gaacgcacag 74280 acgttcctgt cgtactctcg taccacggcc agtttaccaa cccccgcgac ggttaacccg 74340 ccgcagctgt gtcggcgctt agaagcggat tttaaggaac acgtgatggc gtattacaat 74400 aaagcgagct acctgagtac ttacataacc attttaaccg tgcccgctcc tctcccggaa 74460 ggatacgaaa acttccaaga gctagcatgt caatactggt gtggacaatc gagagacgtg 74520 gcggaaatca tgactagaat taatgaccag tatccacagc tgaatctaac aaaagattta 74580 tccggtctcc ttgacctagc ggccctagat caggattccg gaggtcccaa ggaaaacctt 74640 tttacggtgg catctagaat tcccacatac aggtgcgagt ttttgaataa acagtatttt 74700 gttctaatgc acacagactg tatagacgcg tactggaaac aaaacattat cgtgcccgaa 74760 gacgcccaat tgcaaggcct gacggatcaa gatctcacct ccaggatatt ttactgcgac 74820 ctcggcctat ctctacctac gtttaaacaa caaattatgg tttcgcgtca cgagtatttc 74880 aacccaagac tcccagttta cagatgggtg ctggattttg atctaaaagt aaccgaaggt 74940 agacggactc taaacgatat atacaacata tgcgtaacgc tgcgacaggt catattagaa 75000 acgttgcagt taataggtcc actaaaaccc caccaccccg tgtatttttt taagtcggcc 75060 tgtccagccg taacctggcc ggatgacatt tcagataccg cgttttgtca ctgcgacaca 75120 aaaataggga tgagaatcgt aaccccgttt ccgatcggat actgtttggt ggggtccgct 75180 ccacttgtgt ccctgaccaa cattctaaac cgcgtggtta aactggacac gcggctagcc 75240 tcagagtatc ctgggatctt agaagataaa ggaccatttg actccggcat ttacgccaag 75300 gggcgatgcg tgcgcgtacc ccactgctat aaggtgggtc cgggtggcga gctgtcacgg 75360 ctcctaaaaa ttattatctg tcaccccgaa gagtcagata aatcggcgta tttgaaaaac 75420 gcgtttaaag tttctaatct gctacatcac gccccaggag attctgtcac caaaaacggc 75480 cacctggtgt acgcaatcgc tgacgaaaac gagggctttc tagaaagcaa aaccaaaaat 75540 aatcttccaa agacaatcac ggatttggcc gaaaaaatcg agcgaaccac agaaaaacca 75600 ctaattgatt gggcagcaac cgcagtgtgg ccaaaactac acgataccat acagcgtttc 75660 tttccggatg accgcatcgg ccaatttgca tctgtgagct tcatgcactc tggagacaac 75720 attatacaag ttagaccaca aaaaggaaac aactttttct gtattaatca taagcaccga 75780 aaccacactc agactgttcg tgtattttta accctacatt ccacaaaaga aagcgaggtc 75840 acggtgacct ttatgagtca gtgcttcgct gcaaaatgta accataatag cccaactgca 75900 catttttcat ttatggtacc cataacctgc acgtaagaca cacaaataaa atcaccagtg 75960 atgggccagc tctttagctg ctttgtatta atttttacac cgaactaccg cggttttcct 76020 tcgcgaacgt aaacatggca caggcgatgg taagcctgga atacatgaag gatattttgg 76080 acggtaagaa gacctcttat ggctcttaca acttttatct aaaaccgcaa cttaccaagc 76140 ggctcgtttt atacgcttta catgcggtac gtgtttcacg cactaatttg ttttataggg 76200 ggcatatcat catcggactt cgacgactcc tcatcggacg agatggacga cctgtccccg 76260 acgccggagc cagaaccgtc cacggcaccg cacagctttc ctgaaggacc caaatcaaaa 76320 gtggtcgcgt tacctaaaat tcgtaagcga tctaggtcta agacgccggt aaaaattgag 76380 cacagatctc cgcttaaccg ctcgcgatct cgatccagaa cgcgatccgg atccggtcaa 76440 agaacgtcaa gcacatacgt caagagattt aaaccaacgg ttgatgcgcc ccgttctcgg 76500 gaaccgtggc accgaggcgg taagggaaag gccccgttta ttcgcagaaa cgccctggct 76560 gaacgcggac ggcgcacata cggcaacgag catcgcggga aatcagcttt aacgcggaac 76620 attaaagagt ctattaaaaa aatgcacctt ccatccacca tgctctctcg tccacacgat 76680 aaaaaggtat tcgagggact gctgccacga cacctggaac agtgctttca ggtgtgcctg 76740 ccggcgccgc cgccgctgcg acccgaggtg ttcacggatc gacagctcac cgctatagtc 76800 aagtctggcg gacgcagaga cgcgctggtg gcaaaaaaag tcagcctggc taaagtcatg 76860 agcatgtata agcctctgct cacgttcgtg acgggaagaa acaaccaggc ccactggttg 76920 gcgacccgca aaaacacgct ggcgtctgcg ggactcgagg ctctggcggc ctttattgag 76980 gaaggtctgg catgggccca ggtgtgcgta tctcaaaaca gatcgttgaa cgacagcaat 77040 ctagatatca tcctagacag tagtcagagc gtgtgcacgt ggttcatctc aaaaattagg 77100 catttgcaca tacagtgttt cttggaaaat cagggggaga ttagcttggt taaacagcta 77160 acctacctcg tgtgtataaa taaccgcctg gcggaggcgg caaacctggc gggggaggtg 77220 aaactgaatt ttaaattcgc gatgctgatt gggtttgccc taaccttgcc ggcgcttctc 77280 gcagagcaga agttgtctgg cgagagcctg tacctgttta ggtcttttct ggagaaatat 77340 agaccgggag atgtcatggg gctcttaaat tcaatagtgg tggagcacta cacgaaatgt 77400 cgcagcgcgg agtgtgttat tacgacccgc gccatggtag ggtctggtga aaacaacaag 77460 ggactttttt tctttccagc gtaatataac ccatgtgcgt agttacgtta tattatttga 77520 gggcgtttat atgcaataat ccgcataaca aaataaaaga tgtgtaaaac caaacacgcg 77580 tcaagccttt tctgcaaggg ttctgtgcgc gcaacatcta ggcagagttc gccacctagc 77640 ggcacgtctt atatagcctt taaatacgcg gatgttattt acggaagtgc cacatcgaac 77700 cgtggccggg cgcgtaacag taaacctggt ccgtgacagt aaaccgggtc caatcgcgca 77760 atttacacag cacataaaat aggcgacagt ttaacgctgt ttatttaaac atacaacaca 77820 catttcagga gtttcggtct ttttaaaaat ttactttcat tcaaagtgcc gatatatttc 77880 acgttggtgg acaataatgc atattggcgc ttgtgatagg tcctcctcct cgtataggga 77940 ccaggccgcc acccaaatct gtgcaaacgg atcgggtgga ccgggatcag agggtcgggg 78000 cgactgggct aactttgtta tatagtcatc agtatcaaaa atgcgatgtc ccacccccga 78060 tggcacgcgt gttggttcca aggtgtttaa ggtattgcca cgaaaccaca aattaagaaa 78120 tccatatcca ttcatcataa tcccatactg acaactgctc aaaacaatgc cgtcctccag 78180 ggcatttaac gcgttcacaa gtctgctcaa cataacatcg tcatccatat gaggtgccgg 78240 aggcaaccac aactgaagcg gcccgtgagc catacaaacg tggtgttcat ttttatccgt 78300 tggtcttgtg gataaacgaa cgcccatacc ggttctggta aaaacctgtg attgcagaaa 78360 cccataataa tacacctgaa tatgcataaa tccccacggg tcgtcaacag atggcgccaa 78420 acacgcagaa agaccgcttg atacagatag cggcggagtg tgttcctcgg gtaacgcaac 78480 cgcgccccct tcactctcgt cctgcctacc gtcttcaccg gcggtggttg cggacgcctc 78540 ggtggccggg gcggtcatgg tggaggcacc ggcgtgacgg gtacgaagca gcccgagcag 78600 ctgctttacc gtgtattcag ttaccctgcc cacatcgtcg gcgcccttgc gcttgaacat 78660 ccgaaacctc aagccccgca gttctgccgc taccccagaa gcccgagggc acaacctgca 78720 agacatttct tcattggagc gcaacctgaa gaccactgtt gggaatgaaa aactccgtct 78780 caaaaagttc ttttcttcta cgaaataggc actttttcta atcgcgccca ataggcgcgc 78840 cttggcctgg cacagcctag gcctcccgga cggaaggggg atgtttcttt ggttgcagta 78900 gtcctcgtac accttcccat cccgagggta atcaaattcc acagtccacg ctgtcgtagt 78960 tgccagcacg accctggtct tttcgtcgtc tgcccaaaac agtccagaat acgttccaag 79020 atttgcgtga gtgacgatcc attctcgaag tcccatggcg gacggaccac cgctatgagg 79080 tgggcaccag gtagccatgg ctgtatatgt caggttgata ctcaccgctt tcagttcatg 79140 ttaaaataac caaactccgc ccatgcggct acccgtgggc gcagatgtgt gcagccgtca 79200 cgaaataatc ccacctgcgg caactaattc cctcagcgcc cagtcagctg gctaccggtt 79260 gatttcactc acgagcacgc caccccatca tcttcaccgc tcgtgcccgt gtccggattg 79320 tccattgaat ctggtccgga gtcgcccagc tctactgccg ggtcaagcga ttgactcgtc 79380 ccctctccgg gatcttccat atggaaggaa ccggcgacac gagcctctga tgttccaatt 79440 gtcccggggt aaaaacaacc ctcggtgccg cacacagacg aggtttcgca cacgtaacgc 79500 agtcttatgg cgatgggtgc atgggcggga ttcggcgact gaaccgacag acacagggcg 79560 atttgtgcat aatctctagg tgggtcgtct ccaggcttcg gggaccttgc aagagctcta 79620 agataatcca ccatatcaaa cacctgaacg ggctgcctgg acggcaggtc cttatactcc 79680 tcctcattgt tagtaagcac tttcatttcc cggttctcca ggttctttac ggaaatgcca 79740 gtatccgtaa gggcaatcaa cagacccttc tcgcactttt tgtgcatgcc ccttagatct 79800 tctctggcga aactacagtc aacgaccccc ggtggcggta aaaacaaagt cctctcgtct 79860 tgaaaacaac acgcgtgacc agcgaggact ggatatggtc gactgcagac ccgtgttcca 79920 gcgtgaacac gttcgaggcc aacggtcgat ccaaagtata gaaacgttaa ctggatggcc 79980 cctggcagtc gatgctcgcg cacacgcttg ttcttgtcca tccaactccg agccaatact 80040 gtcgcggtaa aaacccgtct cctttcacgt ccaaacccac cccattggtc gtatcggaac 80100 tcactagtta aaccaaggca ctgagtttcg gtggaagaca tcaaattaca catcgcacaa 80160 cttaccaccg gttccggcaa caggcgaaac agtctatatc gagcctccga tcgcccatag 80220 gccttattaa taaatttgag ctctcgtata cttttgtggt gtctcatgtc gtacaaaaac 80280 ctcattttcc tgaatctgcc atagtggggc ggtttttcgc cctgacatat gcctcgcatg 80340 ttgcagtagt catcaaaaaa cttctcgcta tcggaccgag ctgcagttac tttgttccac 80400 gggacccgga caacggtctt gtcctcattc tcccaaacca atccgtggta ctcgctcgat 80460 tcgaccgcgg caacaagcca ggccttaata tcaactccac gacccgccat tccgcgtatt 80520 gggaccttga cggatcagct cttaacacaa atgaaactcg ggcgttcgcg gcaccagtta 80580 atgaacgtat ctaaatgacg gagtcagtgc cctaaacata tggctaagtc tactgagact 80640 gtgcttaggg gaagagtgac aaacacctgg cactcaataa aattttgagg gaggtcattg 80700 acccgtgcct tcctctggtt agtattaacc ccattgccac catattcaag gaacagaact 80760 ccaaatacaa aacactttat tacagataaa aggcgctcgc cggcctcaca aaaccggtcg 80820 cgcgcacagg agacattaaa cattggcagc ggacaacgcc tgccacagac actcgtgcca 80880 cagctgaata attaacggta cagtgctttg caccccaccc tcgggtgtag gtacgccccc 80940 aaaatatagg taaacacaag cttgtggagg cgccgtcccg tcccgaggtg ttctggccat 81000 gcctttcata tagtccacca agttaaatgc acgacacgcg ttggcgcacg acaggaccac 81060 aatcgccccc ggagattcga cgttcccttg aacaaacgcc atggaatgcc ccaaccacct 81120 aatgtaaatg ccggaggggt cggcccaaaa cgccaacccg cgcaaaagat ctttatccag 81180 gaagcgcaaa gcctcggcct gaaactccac taagtggctt ggaatctccg gaaccagtgc 81240 ttgctcggca atcggcgcaa cgcatatgtg cccttgagcg cgacgctcgg acaatgggag 81300 cacgcggatg ccgttgggcg attctgtcac cacttcacca aatctgtctc cataatagta 81360 aaacgttata cgtagcatcc aacactgctc acccccggct cccaccgcac cagtgtactg 81420 aacaccggca ccaaccggac caaatttatt cacggcctcc tcgcgcaacc cccgtaacat 81480 agcagtagta ccggaggcct gatcgcaacg agcacacgac ctcacggtaa ttggtaaaag 81540 gcgaatggtt cggcatctgt tcggatatgg agtcgaaagg tcatcattag tcgacacgtc 81600 cgacacggtt tgactatgcc gtatggcgct ggatagccag tttttgcatt ccttagcggt 81660 caattccctg ccagccgcgt gcaagatgcc cctggatcga cagtagtcaa taaagatgtt 81720 tttttccgac tcctcaacgc ctctgcttcc tctgtcgtga ttccacggta tgcggattaa 81780 agtccgttca tcgtcgatcc accgcatccc gggatgacga cccgtctcgc aacattccac 81840 cagccatcct cgaaggctgg atggtttggt cactcggacc ggccgctcca tatcctcctc 81900 gccgcgtgca cgctaatgcc aaaccttgtc caagttacct cctgagaagc acctgcgacc 81960 ctcacagagc tacgcgtggc aaacgggaac ttgtggtcta gtctgctggg acagtacctc 82020 ggcgttattt ttatctatcg tgcactcctg tggaggaagt ttgtggttta tgcgcaccac 82080 cgggaaggat tcatctgtcc ctgcaccaac tcgtcctgac agaccaccac agaaatagga 82140 acttgtgggc tctcttgggc accaggttgc tgtgagagat acagtgttgc cccgttgcac 82200 ggcgcatggc tctctggtac cggggagcgg gcaagctttc tcatgaaacc catgaaataa 82260 aaaatctgct gtttcgagag gaacatgacc tctcgttgaa taatatcacc attacagtcg 82320 ttacccgcag cgtaaagcgt ttccctgttc ctattatcga cgtacactcc ggtttcattg 82380 ccgtgtacgt agatgccctc gttatacgtg accagcattg tgtttatttg cgttatctga 82440 tctggagtca gttttccagg atctggcgat ggaaaccaaa cggtaaaccc ggtgccgtaa 82500 aaacacagat gaccgggacg tggaaccggg cgcggatgca aacgaacacc tcttcgatct 82560 tgggacgtat gatccagtgc caaaacgcca aaataaaaca cctgaattcg taaccgccaa 82620 aacggcacaa tttgatgagg cagtggcgct tctgggaccc cgagacgatg tgctcgagcg 82680 tatgctgatc tcgttggagg gaccaacgta ggcaaggggg cgggcagcgg cattcctggt 82740 tctaacccaa tgccacacac ctgctccaaa taattgataa tcccttcaga gttctcatca 82800 agaatacacg caaaacatcc agaatccatc aaaggcttta cccggaaggc ggtccagcct 82860 cccccgtgcg tccgcacgac cccgtgctcg cattcttgaa atccagcatt ctccctcaaa 82920 cccctcaaaa atcgtctctt gcactcaaac acgtttccat caatcccaac ctgcaggcct 82980 ctctgcgcgc agtaggcgac aacggctgga gttcctgccg ctcccttctt ccaagacagc 83040 ttaaaggttt ttttctcctg atcgcaccaa gtcaggtctg aataggtttt ctcgttgaga 83100 tggtaaagcg tccacgatcg caaatggctg tagttagaat ctcgaatcgc catggcagtc 83160 cacacctata caataaggcg caatgcgagt ggactttact cccctgatga tattgttact 83220 gctatatctc cttaaaacgt gcacctggca aatcaagcgg ctctatttct gccacttcct 83280 catttataaa accatattgt ttctggtctc acgtttttag ctcacctgca acgacacggt 83340 gaatgagccc gagtttcgct cctcccgtgc tctgaaaaac actggcccag agctaaaaag 83400 tgaagcaaat ggcatagctt tcgatttcag tcaccggcag tgagtggtgg acattagaaa 83460 gtgttttgcc cgcacattca actgcgcact caagcccaac caatatggca cgtgaccatt 83520 cccccatcac aacactagta cagaaaaacg aaaccatacg cgaggtgaca ttctgcaagg 83580 tagaaattta ttaatccggt gcatccatct aacaaaacag caaatgttta ttcaaagtgc 83640 ctatagattt ctgtttggtg aacagtcata gataagggag ccctcgaaac gtttctctcc 83700 tcacccaatg aacaaccaga aacccaaagt ttaacaaagg ccgccggagg atccgtgtcg 83760 tgcggggagg gggacctggc aatatcaagt aagtaacgat cagtgtcaaa tgcccacacg 83820 tgcatcccgg tataggcacg atgtggaaaa ttgcgcggtt ccaccgtatt tccctgaaac 83880 cacacgttag gagcccctgt aatcgtaaac acaattcccc tgctggtgct gcaaaaaatt 83940 attccatcca caagccattt caaggcgtcc tcaagtctct gccccatgga agtgtcagtt 84000 atctgtggaa tcggaggaaa ccaagcctgg agaggcccat ccaaaacaca cacgtggtgt 84060 cctgacttat ttgtcggtct tgaagatagt ctaatgccct gcccggtggc agttgacagc 84120 tcagcctgta attgcccata gtaataaatt tttatatgca tgtgacccca cgggtcgccg 84180 gcagatggcg cagcacacgc cataagtctg gcgcgcagga cccccgacga atatggtgca 84240 tcgtcgtccc gcgcgtcgtc tccaccttcc tgaccttcca aatgccgtgc ctcgtgatca 84300 cctactgacg attctggaaa agcgtgaagc atcccgcgcc cgagcatcgc aaagcgcata 84360 ttgcgcaatt caaggcgaag cgcgtccacg cgcggacaca caggacaaga catctcttca 84420 aatgaacgca acctgaagac caccgcagta aacggaaatt ggtcggtagg gaagtcctta 84480 tcttcatcaa agtacttgct ttttcttatg gctcccaaca agcgtccctt ggcttgacac 84540 aacctgcctc ttccagacgg caaggggatg tgtcttaaat cacagtaggc atcatagtgt 84600 tgaccgtcgc gttgataatc gtagttgggc aacgacggtg atgtggctgc caacacaagc 84660 ctggtcttgt gctcgtctgc ccaaaacaat cccgggtaga agccactgtc ggctttggat 84720 atcagccatt ccctgagggc catgccataa cgagatgggc cccttctcga ttcaccagcg 84780 gccatgattc tgtcagcaac gtttaaaacc catgtgaagt ttcagttcga tttaaaatga 84840 cacaactccg cccctactgt gacaaacata gagaaagtgg cacacgtgtg ctgctttggc 84900 cgttctgtca gatgaacccc accggtaaca tctacttcct ccaatacggc gcgaaagtag 84960 aaacagaggt gctccctgtt gttcccgaag caccgccacg cactccagac ggtccctcgt 85020 ccccgctgtt actgcccgtg gcactgtcac cggtctcgac ggatacatca tcgcacacgt 85080 agcgaagttt cagggcaatg ggagcatccc atgtattttc ggactgagta gacgggcaca 85140 ggaaaatcca cgcacagtca cgcggtggga gatcgccagg agtcggcgat ctagccagtg 85200 cccgcaaata atgcaataaa tcaaacacct ggaactgctg cgtaggctgc agttcatagt 85260 aattttcaga atagttggtc agcgccgtca tgttgcgttc ctccaggttt ttcacgcaga 85320 ttccagactc caccatcaca caaatcagac ccctctcaca tgttttctgc agggcctgca 85380 aatctgccct ggcgaactca catggaacca actgcgccga cggcagaaaa cgcgtcaatg 85440 gattatcggc acaacacagg tgtccagggc gtttgggatc cggaaggcca catattcgca 85500 caccgcaacc ggagcgcaaa atttcaaccc caacgttctc tccaaagtaa aaaaatgata 85560 cctcaatagc tccgggtgca gcctgcgcgg gagagccctg gagcctggct ttccgtctct 85620 gaatggaaac tctcaatggc aacctagccc ttggccgccg cgcctgttca aagaaatcat 85680 ctcggacacc actgcccatg gaacagctat gcaacgatgt ggtcgcaatg aggttacaca 85740 gatcgcagcc atttgtaacc tcaggaagca attgaaagag tctgtatctc tccccagaga 85800 cgcccccggc cttgctcggt ggcgtgagtt ccctcaagta cctgtgagat cttactgcgt 85860 ataacattct aattttctta aatttattgg catgtgcagt cgaaccgctc tgacacacgc 85920 cacgtgctaa gcagaaatcg tcaaatatct tgttatattc ttcgtcgatg cgactgtcgg 85980 tggatctgtt ccacggaata cgtataatgg tcctgtcatc gtcatcccat accactccgg 86040 ggtatcgacg agactccaca gcatcgatga accaggcttt taaatccatg ttttgttccg 86100 ccatctcgcg tgttcaccac ctctaccgag cgggtcagtt aaaataccga gcccacagga 86160 ccacaagtct ccgtgaccaa aagaatctag atctgaaaga agcctaccta tatacgccca 86220 cagggcagct ctctaacaaa taaaaaaaat tttctcagaa aacgaataga ggaacactga 86280 cgacacgcaa tctagtcaaa cccaaaccta aaagccttca ctgacccata tcttcccctt 86340 cccgagcgag tgcggtttct cacatgccat aagcaaacga aaacgctacg cataatgaaa 86400 cgtgagagca aaaaaacact ttattgcagg gagaaggtgc ttgcaaacag tgcacggtat 86460 gcacggtaac agtatgtgtt acatggcagc atccccacac gcccgccaca gacactcgtg 86520 ccacatttga atggacaacg ggatcgtggg acacggctcg ccttccggag tgggaacgcc 86580 tcctatgtgt agagacgcat aggcggccgg aaacagcgtt ccgtgtggcg gggtagctga 86640 caccgcgctc agatattgaa caagcgaaaa tacgcgcgca actcgcccac tatttatcat 86700 atccaccggc tccggcgaac ctccattacc caacaaaaag gctggaacgt gacccatata 86760 ccgaacgtaa atcccggacc cgtccgcata aatcattagt cctcgtataa tctccttcgc 86820 cagccacctc agcatgcttg tttggtaagg tagtaaatta tgtgggttat gcggcaacat 86880 gacctgttct ggcttgatgc ctgcacaaac gtgtccttgc aagggttgct tgggagctgg 86940 caacaggcga acgccgttgg gtgacccaac ctccatgtta ccaactagcc gcccatagta 87000 ataaataacc aaacgtatca tccaacaccg caccccgtcg cttcccacgg caccttcgta 87060 ctccctcccg gcaccaagat acaggaatct cgcggtcacc tcgttgcgta ggtccaggag 87120 catgccaccc gtggcatccg cttcgttgca gagcggacag gaccggacaa agattggtaa 87180 caggcgaata acgcggcacc tgtaaggcgc aggcgccgac aggttttcct cagtggacac 87240 atcttcaacg gtctgactgt ggcgtatagc gctggccaac cagtttttac attctctgag 87300 gctcaatggt ctgttaccgg tgtgtcgaat gcctttaaat tgacaataat ccagaaagat 87360 gtttttctca ttttcagaaa cgccacctgc gccctttaaa tgattccacg gtagacgaac 87420 cagagttttt tcttcattca gccaatgcat ccccgggtgt ttaccattat cgcaacaatc 87480 aagcaaccag gccctcaggc cagacggccg gtttacacga attgaccccg cgcgtccttc 87540 cgccatctct gagggtccgc tcacctaaac tggcttataa aatgtatttc cctttggcac 87600 aagtatttta caaagttaca cctccagcac atacccttgg ctggtaggga aggcacctag 87660 tagctatttt catctccagt gccgcctact agcggaaacc tgcggtctac aaaatccacc 87720 gagccggccg aatgtcacca tgagtcaatt catcctgaca gatcaccaaa atgacaggga 87780 cctggggtct tttacgggag ccagggcgac ccccaaggta aagagtgact gcgttgatgg 87840 gaaccgggtc gccgggaacg ggggaaaggg cgagtttgcg cagtagaccc ataacataaa 87900 aaatctgaaa tttggcacag gatcgcacaa aacgctgtgc gtggtttccc tctgcgtcgt 87960 tcccggcgca ggaaagagtg tgccttgttc tgttatccac atatatcccc agctcattgc 88020 catgcaaaaa gataccctcc tcacaataat ttatgatctc acacacggtt tctctctgct 88080 ctggcgttaa tggtccattc tcatgcggcg ttggaagcca catcttaaac gctgtcccat 88140 aataacacgc atggccagct tttgggtctt ggcgcttatg caagcgtacc cctctacgat 88200 ccacgcccgt gtgttccgcc accagcgatc caaaataaaa aacttgtata cgtagccgcc 88260 aaaatggagt gatctgctcc gggtgtggtg gcgcggcaat tgccaacctg gcggctctgg 88320 cataaacgga ccgcgccgca ccactagcct ccgccggagc ttgaggcggt aggggcgtcc 88380 aaggctcaag tccatgaacg caggctgcct ctaagtaatt tatgacggtt tccgaatgac 88440 tatccaaaat gcaggcataa cacagtggat ctacggcagg ttttaagtaa aaaaatcttt 88500 ctccgccaga atttgtcgtc gttgccctgg tatcgtcctg ttcaaacccc gcgttttccc 88560 gaagcaccct tagcagtctt ttccgacaat ccgacacgtt atgctggcgt ccacactgca 88620 gatccctatc caggcagtac gcaaccaccg gttgcatacc ctgcatacct cggtgccatg 88680 atagcttaaa gctcctcttt tcctcgtcgc accaacgcaa gtggtctgga tacgtgttcg 88740 cttccaaatt ggaaataatc catcttcgca agtgattgtg agtgatttct gactcggcca 88800 tcgtgaacta agttcacgga accgtcgcgg aagcactcag caatccccca aactgtaact 88860 gaattttatg tccaccttat aggatgcacg tgtatgtata tgccccataa aaaaacttgc 88920 acttcctcat aattcacccc caaagcgttt cgggtcaccc accttaacta acccacacat 88980 tacacggttc agagtgtccc aggtttcacc actcccccac cgctacagag aaacgaaacg 89040 ttcaatttaa agggcaacaa gctcaacttt atttaaagag aaaaaaacca ccgccattag 89100 aaggtttccg caggcacaca cccccaagac tattcgtggc gagttcgcgg cacgctgtag 89160 tttttttcta attatttgta attcgcatcc aatcgccccg aacatagtca gtaaaaaaac 89220 cgtaaacaca cacactctgg tgaacaaatt atgcgtccct ggccccaaaa cgtgcgtgag 89280 cgtcagcagc acggccgctg ctaaaacata aacaagggct aaaacgttcg accgaaacac 89340 gagtccgatg caacaaaaaa gcccaacgtg gaagacaaaa aaatagtgta caagtccgag 89400 gagcagaggc gtcgtcaggc caacagacag cgtacccgcg gccgcccctc caattaaaac 89460 agttacgaga taaaagtccc atccacacac ctcaagcgct tgctttatag agtatgtgat 89520 gtaccgccta gaggtgagcg aaaaaattgc atggcgtcgt tgcaggcccg cctcgtaaag 89580 cggatgtgac cgcagcgctc tgagcgaaca aacgccgcct actataaagg ccaccagggg 89640 cagcaaaaac accggggcta gaaaaaggtt cttcagaacc aagaaatagt acaccgagaa 89700 cgctgcgaaa aatccaagtt cgtaatatct atgggcgatt gtggggcaca gatataccac 89760 gtcattcgcc acaacaacac agagcagcag gcacaggcac gaccccacaa aaaaagaaac 89820 gtaaacccac ggaaggtcaa cgccaagggt ggacgccatg gaaccggcgg tgataagaat 89880 cgccgaaatg gtgcacggta catccacctg tcgcgagagc caggccggag gcccaactac 89940 acaaactagc agaagcagcc cgtgtaagcc caccgcgccc caggagaata taatgttctc 90000 aacgctattc aggggctcta aaaaatacag cgagtgataa ataaaacaca aaataaaggg 90060 ggaagccgcg accgtcccgc tcataaaaga tagccaggcg agcgacgcct ccgacgtgta 90120 cgtgcccatg gcgcggtgtc taaaacaacg ggttgaacgt tgcgcgaggc gtcttggttt 90180 ttgcttttcc gcgactgggt gagctgctgt gctttcgctt gccgtgtttc ttttctggtc 90240 gagagccgct cgtccgcagt gatttggcgc ccccgtccgt cggctcggtg ccgtcctcgg 90300 cgttcggaac gcactgctct tttaagtcca aatcgggcgt tcttggaggg gacgggagct 90360 caggaacccc ctcgggatcg gcaccttccg agagattgcc cggaacggca ttattccggt 90420 ccgtcggatc tacctttaat agcattacgc ccaacttgac gtcagcaagg ctatctgtca 90480 gcggcaggcc ctcgacttcc agaatctcgt tggcgtgcca gcggaaacca ggcaaaaaaa 90540 atcccggaat cttacatgcg ttcaatgcgg ccactagaga ctctaaactc acatgagtcg 90600 tcaggtcgct agaaaccaca cccacgtcca gctttcttcc tttagcgcaa gtccacttgg 90660 cgtccggggt gtcaggttta aaatcaataa ttttactgac cccgtcgacc gtaaacgtgg 90720 caactgccag cgtttcgctt aacgaaacgg tgaccacctg cttggccctg gttttctgct 90780 gccttagcca ttttgacaac aaggtcagcg tcttgaccgt gaggaacagg cgattccccg 90840 tcccggcctg ctctagtctg tcgtggaacg agggtaggtt gggttcgtcc acaacgctct 90900 tgtgcacggt gctcgtgtga ttgtccccgt aagcgatggt cgtcctaaca aactgcggct 90960 ttccttccgc gttcgactcg tccccgtggt ggtaaaacgc cacgttcatc tccgtgatgt 91020 taactccaaa catctcacgg gtgtgggtga acgtgttccc aagggaggtg ttccgaaagc 91080 taaagctaac ctcgtccgtc atgtcagaat acaccatcag cggcgccagc gcatttttaa 91140 gccggagacc gaggacgccc gcgtctccaa cgctggagag cacgctgagg acgggggccc 91200 tgccctggcc gctgatctgt ataacgcctt ttttaacgat gcccttaatg tggtcgtaaa 91260 ccttactaat gttaccaagc gcatcaacgt ccacgcgggc gccgtaatga aatgagaccg 91320 gcatggctaa ggcgaaccta acaccccagt acgacgagaa gagaattggc aaagacaaca 91380 gacaaagcac tcaatgttca accttttaat agagcctctg gcccggaaaa tgagtaacat 91440 gggacacatg gggactacag atcattatga acggatgtga catattcaga attatcacgc 91500 tcaaaaaagt tcacactctt ggcgctcgta tacgacaggg gacacgcgtt tggggggcgg 91560 gcaccgaaca ggggcggtac gtttattgac ttcaaaatcc tgtcggctgt ggcttgcaaa 91620 aactgctcaa tgtctccgac gttcaccata gtcacgcctc gactcttaga acgaataaac 91680 agagtctcta tctccacggc ttcgcgaaaa aggccgtgga tgtatgcgac ggagggggac 91740 tcgtctcggg agatcatggt gttgtacagc aagccggcgg ccctggtgtg cagcagctcg 91800 tccctggaga tgtagtcgtt agccaggcac accccgcgca tgactccgcg aaggcgaaaa 91860 agtcctatag agtaaaatga acttataaag tatatccctt cgataaccag aaacagcagc 91920 accttttcgg cccgcgtggt ggccttgcgc actcgggaat gcagccagtc aatcttcttt 91980 gccagggtag cgtcctcgac tatttttttg gcataagtca tcaagtcgcc ccgattaccg 92040 ccaaagaata ggttcaatat gttggcatac actttgccgt ggatgttttc catggctacc 92100 tgttcggcgt aatagtgggt cacgtcgtga ttgctgaact ctttaactag gtcctcgatg 92160 ttaaagttta ccaaactctc tgccataccc aaaaatgtga agagaaactg gtaaaactcc 92220 ctatcggtgg gactcaatag tcgcacctca tcggagtcct cgtgcaggga aatctgactg 92280 gggaaccatc tgttctgcca tgtctcctgg gtgagtgcta aaaagccagg gtggtcgctc 92340 gcgtacagaa accgatcggg ggactccata gcggcggtta ctattgacag gccagacata 92400 cctcggcctg ctcaccgtcg gccttttgta cgcggttaga ctccgcccct tctgaagagg 92460 tgttgtcacc cacgacctga tctaagcact gcagggcatt aagttttgtc tgtttctgaa 92520 tccgacaata atacagcatg gtttttaacc ctagcctgta tccggtcagg agcaagtctc 92580 gaatataact cgcccgcgtg gcctgctcct cctttaaaaa gaaattaagc gactggctct 92640 ggtctacaaa cggagcccgc gcaccggccc gctccaactg tttgattgga cagtaatcga 92700 aggccgttaa aaaaatctta tatctgtcct tcaggggttc tggaaacgaa gccacgtcgc 92760 ctccgtaacg gcgcaccgtt cgcaggtcac ccggcttcac tcgcttaaaa aaagttacgt 92820 ttggttttag aatctcttct ttgctggtaa ccttcgatgc gatattggca aagaacggat 92880 aaaatgcttc ggtgtaaccc gtaagctgag aggttccggc cgttggcatc agcgccaaaa 92940 actggctgtt gaaaattcca tgctgggcga tgctgcgccc cagctgctcc catctttcca 93000 agggcgggtg ggacggctta acgccgtccc acgtttgcca gtgaaacaca ccctgagcca 93060 atcgactccg ctcccatcca tgaaacggag tcccctcgcc aagtaaaaca atctcgtgac 93120 tcgtgtgcac cgccgcaaaa tacattgcct gaaaaatctc cacgtccagc ttggcgctct 93180 cggcgtcaag gtagccaaag ccgagttcgg caaacacgtc ggccaatcct tggacgccaa 93240 tgcccattga tcgttccttc tggccgcgcc taacgctctc ggtaggcgcc gtcccgccca 93300 aaatgcacgc attgacaata ataactgcgg cctccacggc gtcatcgagc agttcaaagc 93360 caaatgttac atcccccttc ccgggctcca caccagactt tcccctgggg ggtctgagac 93420 acttcggcag gctgatgttt gccaagttac acacagaagc ctgaccctcg ggttgctgca 93480 cgatttccgc acagagatta gaacagttta tggcactgcc ttgcgtctca caccagtggt 93540 gtttgttgag cgcctccttt agcaggacgt agggactgcc ggtcttaatg acggtgttga 93600 taagggcata catcatcgat tttaacggca acgagctaga gtgcttgcca gcggccacta 93660 gtctgttgta ttcaatctca aattcggcac cgtatagttt taggagattg ggcgccacct 93720 ctggcgcaaa caggtgccac tggccgtctg ggtttgtttc gtacagccgg aaaaaaagct 93780 ccggcacaca cacgccctgg aacaggttgt gacaccgctc ctgattctcc ggcatcttag 93840 cgttcaaaaa atcacaaatc tgatgatgcc ataattccat gtaggcactg gcaccaacgg 93900 gacggatatt gttgtcgttg aagtacccta cgtgggcgtt tattaatttt aaacagctgg 93960 taatgttctt gtgttccgca aaggacgaga catctatccc cacgcccgac ttgctagcga 94020 gaagggggga catttcctcg tgaagggctt tgagggtttt gttttcggtc gccatggacg 94080 gctttaaaat aaaacagcta gaaagctgac ctccgcgaag cccggctgac cttaaaacag 94140 gcgttgcgca gcacacaatt tgtgacgaga tgtaatggaa cgcgtaacca accaggtaca 94200 tctcgtccag ctccgtttca ctctgcacca ggtgtctgag ggtcttccgc aaacacggaa 94260 attttatgca ctgacaggcc acaaaaacag ccaccctcat aaacatctgg gcaacgctct 94320 caaaaatggg cgaagagcca tgggttctca gcacgtacgt atcgtaaaac ctgacggcag 94380 acaggtagcc gcagttaacg agatttgcgt atgccttgct ctgcttaaag tcctgcaaaa 94440 gaccgtcaag ggccgcttcg tgttttaaca taaactcgcg aacctcgtcg cttagctttt 94500 ccccgaatac cgtgagatag tctttcaccg taaccagaca cctgtcctcc attattctgt 94560 gccatagaag accggttagg gagttggcct ctacgtccca tccaagggtc gcctttaaag 94620 aattcacaag tgattcggcg catcgttcgg ggtcaaggct tgagctacac cccccggttt 94680 ccgcgttggt aactagggtt aaaggtttgg cagatttagc cgcggagaaa gaagtttctg 94740 tgttcattgt ttaaagaaat agcttccaag accccggatt ggaaacaaac tccgtaaatt 94800 tcaacaccgg tagagcagcg cctttaaagt gaaggctttg aaaagatggt tgtgaaccgg 94860 aaggcacgct tccaagtctg caaactacgc caaacgcaag cctatttata tacaggtcat 94920 tctgcagctg aatgtatttg gtgcgaatca cgccgctgta aaaatccctc aattgggcag 94980 ctatttcaca atatccttta ccagacttaa aaaacccaag tcctagcgcc ggcctattat 95040 ttgccctgat gtaggttaag caaacataaa tagacgagtg ggcggggaga ggttcgtcgc 95100 gcaggctgga cgggcatgag tcatctaaat ccacaaacat gtcactagga agcgtaaggc 95160 caatatgtgt aacaacaggc tctctggcga ctacgtcgcc ctttaacgca gacgtcacct 95220 tggtgacaaa cgtactgtgg accgtttgaa ccaacggccc aaccggcgca agaaactggt 95280 gaagcgaacc ggtttccaac aattcttcaa aattgggtat ggcatcgagt agaccgctct 95340 cgtggccgta ccaaacacac gctattctat tggtctgggg ggcagagtcc gcgtccatcc 95400 tagacagtcg cgccagcgac gtaggcgtga ataacatgtc aatggaggac cccgtgtcgg 95460 tttgtttaaa ggaaaacagg taggtgcccc gaggttcctg tgaactcatc gtctgagaat 95520 aaatcaaaaa atctccgtac gtttgacatt taggcgagac agataaaaat ccatctttga 95580 tggcctccac cccagtggtg gtcgacacca catatttaga gagcagatca cgaacaccct 95640 tagaaaagtc gcgaccgcga gataacgaaa cccggtgagg aggcggcggc agtaaacgca 95700 tcaagctatc attcagcttg ttcacgtttg catccctggt cttcatgacg tcgtcaattt 95760 ctgccgcgcg ggcggataac ggtgacgaga acaccggtgg actttacaga ttaattgaca 95820 acctcctaac gtgcaccgga tctctacaac agcttaaact cctgatggag ttccaactaa 95880 aaccactacc aaccgctcac cttctaagca tgcccaccgt gacccggttt ttaaatactg 95940 cattcaaaat agacaacccc ctggtttcat ttattcaaaa acaccctgtg ttttttttga 96000 tgagagtcgc caggcttccg gatccagtca ttacagacca ccaaagcgca gaaacgtcga 96060 caggcatact atccgaggtc gtgaatgttc ttaatatagc tattcaaaaa ccacacgagt 96120 ccccagcggc taaagacgac gactatctcg acaaccgtgc catattgacc atgatcacag 96180 aatacatcca tcacgtaact tcacgtacgc cctcggggat cccaccgaca ccgccaatgg 96240 gaatcagcca tttaccgtgc gtagagcaga tcctacacga aacccaccgg caatattgga 96300 acctggccct cccggagtcg ctcttcatcg acaccggcga ggtcgcgtct ccgcttcaga 96360 cgtggctaat catatcgtat tgtaaaaaac tgcaactggc accaccgccc ctattcccac 96420 ccgccgacga actggcccgt cgcctggtca ccggccacca cgaactgttc gtccccctat 96480 caacgtcact ggaaacgtac atcaccatgc cagtgtcgaa acggcgagcg tttgagatat 96540 acagcgtttt tgccaaatca aaaaacatag tcgacggtac accgattcta gcgtttaccg 96600 acacggaact taccacgttc accccagaac tgttgttcct ttacgacttc gtaattgaat 96660 ccctgtgcaa aaaccaagca tacgggtgtt cgcgcaacgc aattgagcat tttattaaga 96720 aaggtattga ttttatggct gagttggggg cgttcatcga aaaaacatgt ggttatcgat 96780 cgaccgtaag cctgtccaac gtaagatccg tgaaggccag gctcgcgagc tgtggactat 96840 ccaaagaagc gtgtgaagat ttccgcacaa tgatactgat gacacctcac gagacgacgc 96900 caaagtggga aaattttacg gactttttag aaatggtaaa ccagttaaca ctatacgggt 96960 tctattttta cgagtgtctt aaccagtaca gccccactag catatcgctc gcgaaaattc 97020 aaaatatctt gaaccgagtc gatgccgaac agagcgatcg cgccctatgg cgcactccat 97080 tgatagggtc tttcccgttc ccctggaaat taaacaacgt gctggcgttt tttaagccta 97140 gtgcccccgt ggcaacgcta caaaaaatct acaaggcaat accgtcgtac ctaatgaggt 97200 ctttgttcga aatagcggcc aacaaatcgt ggggtaacat cgcgcttgcg gagagagccc 97260 cgctaaccga catacagacc gccgaaccag accagggtcc cgtccctacc caggttatcg 97320 caaaatattg cagccgtctc cagataagcg cgacagatta tgacgcagtt atcgtctcca 97380 gcccgggatt tgccaccgag ttcattagaa caaaactgta tccgatcctt agcgaggtgc 97440 tccgaaacac gtccaaaaag aatcgatcgt tattccaact cagatggctc atcgtcttcg 97500 cggcagagga cgccaaagac ctagccccta tcagacgctc gttggccctg gcgtactttc 97560 aaataatgga cattttggaa gaaaagcatt ctccggagtc gttttacaac ctgctggact 97620 atcttcagga cacatttagg tgcatacgac aggtgatacc ggaagccacg tgcccacaag 97680 aatttctaca atacctgttt acttttcaaa accttccaat agcggctagc tttattcaga 97740 catccatgac ctttgtagac gacctgaaca acggcatccc cggcatactc gaccttgtct 97800 ccttaggtgc cgcgttttat aacatgaaac tactgtacga ttcaacgcta gacaccgtcg 97860 agattccaac ggaagaaggg caacccatcg tcgtgagcat gttcgtattc aaatccacga 97920 ttcgcatcct cgaaaagctc ttgcaggaag ccgttatcgc gttagctcaa acgtctgaac 97980 cgatgtacgc agcgcacatc cgtttgatgc agcacctcac gtacatgcaa aagatcgccg 98040 gacacgaaat aatgaccaca caacttccat ccgtgtttca cgaaatacac gaggggtatt 98100 tgcagtgttt taagcgtttt aaacgtctta tgttacacgt tacgggcagc tgctgctact 98160 cactgacgcg atactttgga ttcctatacc agccacccct aatacccgat accatcgtac 98220 aaaaaatttt aaactttaac gacaaaacgg acaccaccga cgacatctta aagagtctat 98280 cgcagcccgt gggacaagaa cctttatcgg ctgaaaacga aagtagcagt cgactctcaa 98340 aaaacgacgt tgagctgctt caaaaactat acgacgactt tcggaacggt tccacaaacg 98400 ataaccccac ctctattaaa cttgaatatt cgggtaatta taacgaaaca caagtgtccg 98460 tggattggag cacatataac ctggtgacat acaccgcacc cgacgatacg ttaaaattca 98520 ccccggtcaa cacagaggca ctagatcgca tgcttgcgga ataaacaatg gaattgccgc 98580 caattttttc aaaatttaaa atagagggcg tggcaacgac acaccaggcc gactgcaggt 98640 tcggacaata cgccggatcg cagtgcctaa gcaactgcgt tatctacctc gcacaaagtt 98700 atttcaatag agaatccccc gtgacagaca cgaacgacct tgatgacgtt ttacggcaag 98760 gggcgacgtt ggactttata ctaagacggt ccgggacgct cggctacaac caatatgccc 98820 aactgcacca catacccagc tttattaaga ccaacgagtg gtccgcggcc atcttccaat 98880 cgcaggagta ctttggcctg attggactcg acgcggccat ccgcgaacct ttcattgaat 98940 ccctaaaatc aatcctgacg cgaaattacg ccggcaccgt ccaatatttt ctgtttatat 99000 gcggcgacaa agccggagcc gtaattatca aaaacaaaac gttttacctg ttcgatcccc 99060 attgcgtacc ccacgtacca aatagtccgg cacacgtaat cagttcggca gaccccaccg 99120 ccatactaga gtacgtgtca ccaccagaca gagaatacac gggcagtttt ctatacatca 99180 tgcccagcga atatgtcaat ccagagcact acattaccaa ccactataga accataacgt 99240 tcgccaaagt gcacggcccg cagatagata tatccaccgg catagagccg tgcaccatcg 99300 aagacatccc aagcccgccg cgatcgccgg atgtgacgtc aaaatcatcc aacctcgcac 99360 gcgtaccaaa aaccaccacc gacacgtcta gcgccaaaac cacaccggca ccgctatccg 99420 gtctactggg cgtcgaacca ccgacaagct acccagaccc ggcagccgac gacgcggaca 99480 caaaactctt aactcccgct ccagcgcgaa ccgccgtcga ccaccccgaa ttccaaacaa 99540 caccgggagc cacgctactt ctttcagaac tgtcggcatc caggggtcgg aaacgcaagc 99600 tgtccagcct tcagcgatat tcggattccg acgaagcgtc gtctgacgac gaaggggccc 99660 cacgtaggcg cgcacacgac gatgcgatat ccgccgaggt gatctggatg gacgacgata 99720 tatctcctct atattcaccg tcggcgactc catcgtttga cgacgtgttt gacagccccc 99780 cgatgagccc ggagttcacg tacacgaacg cgacagagga cacggatgga gcgtttctag 99840 aacagatcgt tcgagacgcg gaaacgccgt tctctgcgtt caacgacctt atatcggacc 99900 acgacttttc ttccctcgat aaaaaaatag aacagttaat caaatacgaa gcaccctcgc 99960 agcacctacc gaacatttcg gacaaacgaa acgggcgagc cgtccgagaa gcggcggccc 100020 tccaggcgat ggacaaaatt atgattaata tcatactcga acacggtcta attacagacg 100080 cacaggcccg gggaccgtcc gcctgcaaaa acgttcttca attttttatc ctgtggggag 100140 aaaaactcaa cataccaata agcgacgcca agcaggtcct agaactcgat ctgcaactga 100200 taccgttaca cacggcactc agcgaaggaa aattcaaaca gggggcgttc aaaaaacacc 100260 taacaactaa aattaaccgg tgtctggcgt caatgagggc cacacacgcc aatgcgcaca 100320 aaaaactggc atcggcgttc aacatagaag gctcacagat ctcgtccagc gaaacaaaaa 100380 tatcagtccg ggcgctaaag gaacagatcg ccaaccacct aagtccaggc tttttagcgg 100440 tctactccgc ggacgagcta aaacatctac gggataaaat tcgggaccta aaaacaggca 100500 tcgagcagcg caacagagaa atccaacagg aggaactatt ctttggcgcc gtgctcacag 100560 ccctggacac gttccaaccc cctccgaaac cggcatatcc aatggagatc tttccgcacc 100620 gtaaaaccga cgttatgctc aaccacctag cgtccataac caccaggtta accgatgacg 100680 ccaccgaagc cctcaacaat tacctagaga ccccaccaga tcaagggacg cacatcacca 100740 acatcccaaa cttttcatcc atcgtggcaa atatcatatc cacgataaaa atcctaacgt 100800 acgcagagaa cgacatgcaa ttaaacgtaa cgcccatggc aacgtacagg cgtcagctgt 100860 tgtacctcgg aggcgagtta gcaaccatct tcaacctaga gtggccatac gaaaccgtgc 100920 cgccggtcca agaactaccc ctcgtagcgc gggcaaaagc caaaatggaa tcggtaacaa 100980 agatggaaaa gaaccaacag gctctcgacc agatactagg agacgccgaa acgttactgg 101040 acactataac cgccacatcc ggaaatgaga acccggtccg cgccatgtcc ataccgatat 101100 tggagaccta tattacaaac gcgggcgccc tgataggcac ttctcggaac ccgcggttcg 101160 aaaaactcaa ggccgccatc cacgacctgg cgtcatcgga gtcgttcatt ataatgctgc 101220 taaacaacac acggctcgat aacatatcag acaatctggc caagatcgac ggcatcctga 101280 ccaacaacac gcgttttctt tcgaccgcca ctgttacgaa aacgctccaa acgctgggaa 101340 gcagcctgat acgcgaatgc gtagaagcgc tagataaaag gagcccatct tccctgaccg 101400 acgcgcgtct cctcgcggtc caaaccatac tagggcacgc gtccgttccc gatcacgaga 101460 cgctaacgcg cattgtgtcc ggtgttgcca gcgcacaaaa ggaatccgct ggcgatgatc 101520 cagacaggtg gacgcgtgtg accggtcacc taaacgagct gaagctcgca gctacccaat 101580 cgaacgtcga caaagccacc aggcgcaaac tgttaatgat aataacccgt gacctcaagg 101640 aggcggaggt gtctcaggaa acggtcctgg aaacacggtg gcaagaaaac gtgctgaagt 101700 ttcaaccgtc gacgtccaaa gaaatcgaag actttttaca gtcggcaccg tcagcgaagg 101760 cccgaaaatt tgcagaaaaa cacttacgga cgctgatcgc ccaattcgac ggccacgagc 101820 aacggccgtc cgaggcaacc gccgttccca tggactacac gccaacgccc atacccacgc 101880 cacaggccgt ttctacggct accgcggaaa agggaaaggc cgcgtggaat aaaattcaac 101940 aggcctttca ggatttcaac tttcacctca tcgacgcctc ggattggcaa gaaatggcct 102000 cagaatactc cagacacggc tcgtcccttc cgggtacggt tggaccgaag ctggtacgtt 102060 tcatggagag catctcgaac accctggacg acatcctcac gcaaaaacta gcatctctgc 102120 ttccaaacgg tcccgcattc agacccccgg cgttcgactg gatcgcgcct tatcaaacac 102180 gcgtaaacgc gtttctaaag accataggcc tgccaatggt gcgcgacctg gcggacaaaa 102240 tccatcacca atgccaaact gtcagtcacg cggtgcaatc cgcagacctt caacaggcca 102300 cggtggggac gagtttagaa cgacccgcgg ctgagtactg tcgaatactc tctgacatgc 102360 aagtcgcttt caacgaccac ggaatcgccg tgagatcgga ggccgcggcg tacacggacg 102420 caatcaactc gcctgccaat gtcgcgactc ccccgaaacc caacctagaa gcccccaaga 102480 agctaatgac ggcaacggac gtcctaaccg tcgaagactt tccagagttt ctgaaaacgt 102540 caattctcca acaggaacag cgactcatcg cgcttcaaag agctgaattt caacaactag 102600 aggccagcat ctcggcggcc gaacggctcc gccaatccac gcgtaacgag atcgcaggca 102660 aaatggcaac cgctatcacg caactcttac cccgggcccc cgtcgcgata tcatcgagac 102720 cgttaaactt atcaaaacct atagactttt tgagttcaac ggtatacgac aagattctgg 102780 acaaggagcc ttacgagaca gccatagctg gattcgcgtg gctagaaacc gcgacaaaat 102840 ccgtaatggt ctacagtcac caaaaccaaa cgcaacagtt aaacgtactg ctgagcgagg 102900 tcgaaaaaca gagcaccatc gcccagcgtc tacacgacct ggaagtgtcg gcgagaaaca 102960 cggacgacgt aaaggtgctg aagcaggcgc tagacgaact cgcgcccctc agggtaaagg 103020 gcggaaagac caccgtagac gcgtggaaac aaaaactgga aagcatagaa tccctgcttc 103080 gcgccacgag gacggccgga gaaatatcct cagagctcga acgcatcggc gcgcaggcgg 103140 tcggcaccat cgccgttcgc gatctaggaa cgctctccga tcaatgccgg gaagccgcaa 103200 attttctcaa acaggccagt ttaccggaag gcttctcgga cataggcaca aaactcagcg 103260 agcttcaggc gtacattaag tacaaaaaac agtttctgga gcattttgaa acaacccagc 103320 ctaacgtctt tcgacgcttt ccgctatccc aaaacataac cgaaaacgtt ccggcgcgcc 103380 tcgcgatgga ctcgatggcc agactagcca atcaccttca cgtgcgcggc agcgcgcccc 103440 actttacaac gtggatagaa acgctgccaa ccgtcgatcc tgaaaaaccc actcacgtcc 103500 cagcccacgg aggcgcccct ctgcaccgcc aaatcacgta ctccaacgtc ctagaggcgt 103560 tgttttcatt atgttccacc acgctgaccc cggttccaac cgcccccggt ctggaaatcg 103620 caaccagggc acgccgcggg gcagaggccg caacgtggat ggacagacag tggcccgata 103680 tagctcagac gctccaagac gtcctcgaca cgtacgaaca caccaccacc cacgcaaacc 103740 gggatgcgac atctaacgcg ttcttggcga tgtgcgtgtt tacacaaatc atcaggggcg 103800 ccagcagagc cgtgacgctc ccaaagttac cgggtaccgc cgtcgatttt ccagaagaga 103860 tcgttctaac acccagggaa tgcacaacac tggtcaccgc catgtggccc accctggcgg 103920 ccgcaatctt acgattaaaa tcctactcgg aagccctggg actaatgagt cgtttcctcc 103980 cgctaatgtt ccaggcgctg ccgcacctga cgctagaggc ccaggtccaa aacggcccac 104040 ataacactcc gcctcaggtg agatgcttcg ccagaacgga ggcgattccg tatttcccgg 104100 cgcaatggca gtcagcgaac ctagagcaga gcctgtgggg acagacggac tttttgcaaa 104160 tctgcgataa caatcaacgc aaggccaggg tggcggccgt cacctgggcg ctcacaacca 104220 taaacggcgt ggttttggac caactgtggt ctacatttaa acccatgaca gccgcgtcag 104280 acgacacgta cgtcgaccta gtcaagaccc tacacctgac cacctttggt ccgcgcggtc 104340 caacaccaag gcgagaaacg accaccgagc acccgccgta cgagtacgga cagcccacgg 104400 gctactgcat ctcgggccaa tcgaccacgc cggtccaggc ttcaaacacg ccgggtgtcc 104460 gcttttgagg cggtgctcgg agcgatggtg tttcacgtac caatgagaat ctttttggcg 104520 gcacgcccag cgcctgggcc aggcgcgcgg cggcatgggg ctcctcacac ccatcctgga 104580 atgcgtaccc gacgtcgagc cgtttaaaag cctgtataac gcaccccgca aacccgtgcc 104640 cattaacacg ttacccgcat ccctccaccc ccacgacgag caacaggttt ttctgagaca 104700 ggcgcagtgg ctatcctacc gattcatacc acacgaagcc gcgcggtcgt caagtccgcc 104760 gcttctggtg gtcatagacc cagaaaacct cgtaacggca acgtactcca gtggcggacc 104820 tgcaaatttt gagagcaggc cgttttacgt aatgcccgga ccatacccca cagactggcc 104880 caaaacgctg tcggtcacat caaacacgtc cgtgacgcac ctcagccacg acgagatatg 104940 taacctgttt actacgctat cccgggaaca cgggaccgtg caaggcaggg atatcttcgc 105000 agcggctccc acaaacgtca caccggaacg aaccgccaat catccgacat gggaaacgga 105060 aaaccaatta acaacgcaaa cagaacccgc cgaaaaaacg catgtaattc cggcgtctcc 105120 taaagcgcga acagatccaa tagcggaaac cacggcccac cattcacaag ggcaagcgtc 105180 gcaacacgca aacaacgtaa accagcccgg tcaaattact tcacacgcct cacgtaacaa 105240 accgtcaacc gcgcctcagg cgtcatctcg cccggagaaa ttaaacacgc agacggtgcc 105300 tcgactaata tctcaaacgt cggaaacggc ccatataaac cacccagcct ccggccaagt 105360 caccgaacca aagggaatct ttgggacgta caaaccccga gtgctcaccg agcccgccaa 105420 acccgcacac gccagcatag cctctcgcca accagaggca accaccacgg tccccaagtt 105480 accgattaat gcacccaccg ctaaggtctt tataggcacc gcgtccaaat tcttgccaga 105540 cgtcgaagag agccacggca ccacacccgg cgcgcatcaa tcaaagatag atcaaaaaca 105600 atacggcgaa agtcagcctc accgcacccc acaccttgaa gaggttccac gggcgcctca 105660 cgtcgacact ccaaccagcg cacacataaa cgtcccctct agccaaggtc caaaaacaat 105720 acacgcgcgc gtaacacccg gtattcaaac agtaactccc agcgcccccc caccggccgg 105780 tcaaatccgc gcattcaata cacgcttccc agaaccgacg gccggtcgct ccacgacgaa 105840 tcggatgtgg aattgacccc aaccaatgcg gtaaaagaat tgcccaaaac acaaaatgtg 105900 tctcacaggc ccgaaccgga cgactataaa tggaccgccc cattcggtcc aaccgtagag 105960 attcatcgac tagaacaccc ccaaattctt gaaaatataa catcactcac cgtccccact 106020 cccagagtca ccccaatccc tcccactgac gtctggatac ccctatccca cgttaacatg 106080 caacacgaag aaatttcgag agccaagaat gtgttaatgc gatttattca aaacgtacga 106140 agaaaaattc aagcgtcgtc tgacgctcta tccgaggcta ttgccagaat aaagttttta 106200 tatctttaac gcgcccatct cacttgctct ttttgttttg agacgagcgt cttgtgtcca 106260 gagtagtcgc gtcgctaggt gataacgaag tggaccctat gccagaagac gccacgctcc 106320 cgggtccacc gccaccgggc gtagggccaa ttgagcctat taatgaatgg ggcccgctgg 106380 agatcgtagt gaagctattt gacccaaggg tggaggccac cggggcaacg ctcggggcgg 106440 cggagccgga cccggacaaa acgctcgaga tactagaact agcgtccttt ttgccgcgaa 106500 ggccccggag gtggtctttg cgcaaaattc cgtttttctt ttgcgtatac atgtcgtaat 106560 gatgtttggc cgttaaaaac accagataat tacgtttcgc aatggcatac tgggcgggag 106620 acatgtcacc ctggggaagg ttgttcatct cggcaaccag cgggtgattc ggatagtcgt 106680 gctccagtcg tccctgaaca atcggctcct taacccgcaa tgacgacata tcttaactcc 106740 tattgcactt tccacaggac agggacgata tagacgaggt caaataaaac agctcggcca 106800 cgcgcaaatg ctttaatagg ccggtcgcac agtccggcga ggccaaacag ggcacaacaa 106860 cgctaaccaa agagttcgcg tctcgtatgg agtgtgccgc gttgttggcg agcacgcacc 106920 gtaaataggg atcgccaaca cacgtgatct cgaatagaga tataacccgc atgtgcgatc 106980 cgccacaata agagcaatat acgcgcccgg tggtcgcgca gatcgaaagc tgcttttctt 107040 tttggtcgcg actaaaaaac acgttggtgg gtgggaaatt tacggtttca aatttacccc 107100 gtccgaaatt caaacagtaa ccgcactcga ggcataccac caccctcgga gcgggaacgg 107160 ttttttccag aacgctccta gccaccacct gggaccaaac aggtagagaa atacacggaa 107220 acagtacgtt gtacgccaat actttctgac ccaggtcgcg ggatatctcc gtctcggttg 107280 actcccctat gggcagcaca acccgggaca tgctcaacag gcccctaaac gtcaggctcc 107340 tcagaagggc gttaaacggg ttgccgcacg ggacggttgg cgccagttct cgcagcgagg 107400 ccagcagtcc cgcgtccgaa gggcccaggc cacgctcatc caggttagct cccaaacgtc 107460 tggaaatgga cggaacgttc agctgcatcg cgacacaacc ggccccgttc catttcttcc 107520 gcaaaacggg caaatccagc gcgtgctgtg gcgaacatgt aaccagggga aaccgctggc 107580 gacagttgag ggttttgcac acaaaacaac acgccctcgg aaacgacacg accagatacc 107640 tggaccatgc gcccctggga acggccgtta aacttagacc ttcgttgtcg gcatagccca 107700 cgccggtgca gatacacctc agcacccacg cgtacgcctc caacaacaac cggccagtat 107760 cgtgcagccg cgatttcaca tcgccgtttt taggcgggtt atccggcatc cagccggtag 107820 cgatatcgtt aagggcagtt tgaaaggatg gggcagaaat taacgtgcgc gcccattccg 107880 ggggttgccc ctcccaggca ccgagcccgt atgtcacaaa acacacgtag cattcggggc 107940 acaggccaat tgcgcgcata gaggccgcga aatctaagcc cagccgagaa caatccagcc 108000 aatgatggac aggataagga acgcgcccat gacaggcagc ttcgtcttca gccaagtcag 108060 gcaagcgccc cgaggccatc ccccaatagt accgatggaa tcggttaatc ggtcattgcc 108120 gcaccgctct ccgctcccaa tatccgtcaa ctccgacccc gaggggcggg ccacggagcc 108180 cgttcgcctc aacgcgccaa ggccgtcgga gtgccccgta agggcaaaaa ccgtcctaag 108240 aagggttttt aaccgtttag cgctcttcgg agtcacaacc aaaaactgta agacctgtcg 108300 gtgctccgta aagtaggtac ggcatataac catggagctg taaacgttta ggtctccgga 108360 gaaaaccaga cgtgccttaa atttcataaa atcgtcctgg cccaggaaca cggacgagtt 108420 cctctcgaga tacacgtccg aatttatagg caggtttttt ccaaactggg catcggcatc 108480 acgtggctta cacaaaaaac acttcagcgt ggtggccagg ccgttgttag taattacaaa 108540 acacggggca aacgggtagg ccagcctctc tagtttgtgg agccaaaact tatacacaaa 108600 ctcgagatga taaacgcagc cgtgctgcag gcgcacggtg cacaccggga ccgccccgcc 108660 tttagcgtat acgggagccc cgtcctgaca cctctccaag tccagagaaa ttccggaggg 108720 tcccaggtaa gagacaacta catcgcacag ctcgtcaact aaacgtttcc cggaactcat 108780 acttgtaaaa atcttttagg tgctgtgcgc ggctcccgta aaaaccgcgt ccgtgctgac 108840 gattttgtga atgacctgtt ttacggcgtt caccttggcg tccagaacca tgcagtgctc 108900 acagtgagct gaccgcgtct gagcacgatt acaaaggaaa gtttttaaat actgacagta 108960 gttaatggca ttgagcctgg agtatatggt gggaaacata attttcatgt cttcgggcag 109020 cagggactca aacgccaata aatcgtcacc ggacatcacg tgagtggtaa agatgcttac 109080 cgcgggtacc gcttagctca cgaacatcaa accccttcaa atattttagc cattaaaaaa 109140 ctaacccacc ctaaatccgt ttaacacaga ctaaacgctc ctaccgagca tgttcgtgcc 109200 gtggcaactg gagaccctta tgaaacactg gccctctctg cgggaactcg tagaacaatc 109260 gttccttccc ggaacccccg atgtagcttt taacagccca gtattgattc acactcagga 109320 ctctctacag cccgcctcat cgtgcagggt gtgtaacatt ctgttcactc tggtccgaac 109380 attcccaccc cccgactctt tctttgaaga ctacggctgg ttgtgtctca cgtgcctata 109440 cgccccccga tcatggacgg ctacacttat ggtggccgcc gaccttctgg aactaataca 109500 catgtacttc ccgcaacgcg tcaaagatgg gccagtttac accacccaaa acatcctcgg 109560 aatcgacgtc cagctccact tcttcgcaac ccgctgcttc cgacccattg acagagaaca 109620 aatactccac acatctcatt taaatttttt acaaaccgag tttattaggg gcatgttaga 109680 aggcacaata ccgggatcgt tctgttttaa aacgtcctgg ccgcgcacag aaaaggacga 109740 ccaacaacct accgttgcgt gttgttccgt tggccgcgga aatcacgcca accgagataa 109800 ccacctaccc gatgacctag aagaggcgtt caactccacg aacgccaagg aaaagcccag 109860 catcctcggc gtcttttcgg caacgtggtc agaatcccag cttctcggct ccgacacaca 109920 acaggcaact atccattcac aaccctccac cttcccaacc ccagaagatg ctgaccaatc 109980 acagggcccc tgcctaatgc acccaacact caacctcaaa acaaaaaacc acaccgcatc 110040 catctgcgtt ctatgtgaat gtctggccgc ccacccggac gccggtccgg ttctgagaga 110100 tctgcgtcgc gacatcctgg aaaacatgga aaacaacgtt aagctcgtta atcgcatatc 110160 gtacatccta aacgatccgg actccctgtc acacgtgcgc gacgaacatc tgcgcggcct 110220 aattaaacgg tgctcggcgc aagaaatcca caagcatttt ttctgcgacc cgttgtgcgt 110280 cctcaacacg tactcgcact gtcccgcggt tttatttaaa tgcccacctc ccgaaaagta 110340 taaaaagctc aaagctcgtc tggcgaccgg agagttccta gactgtaaca gaatatttga 110400 ctgcgaaacc ttacagaccc tggccgtcct ctttaagggg tctcaactgg ccaaaatcgg 110460 caaaaccacc tcgctcgaaa taatccgtga actcggattt caactccgtc gacacaacat 110520 tcaaatcacc cacccgtttc aaacctccaa cctatacatt tgattttcag aagcgcgtca 110580 gacaatgcca aaacagccca gacgtcgatt ggcgtctcga acgccatacg cacctagcgt 110640 caagcgaccg gacgggcccc agtccacgca accggcatcc aggcacggca gctgcaaaag 110700 cgaaattatg cagtggaaaa agttagtttc agacacgcag tttttttccg ccctaacgcg 110760 ccgccacgag ctgggggtgg actttttaag agaaatgggg accccgatat gcacctcaaa 110820 gtccgttatg ttgccgttaa acctaaaaac catcgccccg ggtcggtgcg tgtctctctc 110880 atcattcgga cactcgtcaa acatgggatt caactgttcg tcgtgcacac caactgacag 110940 gtcggcggtg tctctggacg caaacgcgct cggcgaagat tccgccagaa aaaacagtga 111000 gctgtgttca gtggcgttaa ccttttacca ccacgccgaa aaggtcgtgc agcacaaggg 111060 attttacctg tctctgctca gccactccat ggaagtcgtt aggagaagct tcacgcaacc 111120 cgggttactt tacgcccacc tagtcctaaa aacatttggc cacgatccgt tacctatttt 111180 tacagtagat gccaatgaga gacttgcact ctgggcggtg tttcacacta gagacctaca 111240 cctgggggaa accagtctgc gactcattat ggacaacctt ccaaattatg acataacggt 111300 ggattgcatc aagcaaacat acataatgaa gtttacaccc tcgcgaccgg acaacgcgac 111360 cgtaacggtt ccagttaata gcatctgcga ggccgtggcc acgctagact gcacggacga 111420 gtttcgagaa gaaattcaaa ggggaacaac cataataaac tctcagggct cattgtaatt 111480 ttcccctaac tggcacaaat gtaaaacacc taaccaaatg taatttttat ccaaatgtaa 111540 gttttttaat tttgtacagc ttaccaataa aaataacttg tgtttacacg aattgaaaag 111600 ttttttaata tcacaataag taaacacggg aatagtaaga acagaggtca acgaaactaa 111660 aagcgttatc tggataggat ccctagaaag caattaacgt gcgccggtat caattaacgg 111720 gaacgcacgt taactgctct ccacggatcg caacgccaaa ctccgcgttt taaggaccat 111780 tcgatgccgt taaagattgg cggtaaatcg caaaaggtcg tacatcgtag tactgatttt 111840 acgatgtgca cacctttccg cggttcaccg ccaacaacaa aagcagttca cctgggcacc 111900 caaatcgccc gggcctttta cgccaacgta caaaagtgac tggcgttcta cgatcacgag 111960 caacactatt gctcgcaaac acaatagcgt tgttggtgac cgcaaactgc caaatcctga 112020 tatgcaggga catggtcctc aaaatctaaa acggacttcc caaaaaaaaa catgcggcaa 112080 taaacaaccc ctcgcggtta atgcacatcg caacgaaacg gaatccaaag aacacgcccg 112140 atcttaaaac cacgggcacg tgtctttggg ttccgggggc gttacgatgg aagttcgtca 112200 ccagatatcc aacaaacctg ttacaaaagg gtaaaaataa tcggttttaa aataataaac 112260 aataaaaaat tagccgccga agttacattc cgacatacaa gcggacccaa aaaaacaccc 112320 caacgcaaaa caactggaga atgtgtcttt gggtcccttc cacgtcgcaa tgaaattcct 112380 ggtgaacgtg tgctgcttaa cgcgttacag ttatatttta tggctacgta aacacaccaa 112440 tctaaaatgc taacacgcgc accgcgctta ggcgcatctg tgcaactaac tgctgtcagg 112500 ttactactct tatttttaac aagtagcaca ccaactgcaa ttaattgcac taaacccggt 112560 tctgtcttct tttggttaag ttggcccaaa gtctttatgg agaaccatta ttcattcatc 112620 tccgttaaca gcgttagcat tactgttgtc gctgcgggca aaataagttc gaggggaaaa 112680 acagcaacaa attgttagtt taaaacaact caagttctaa aatctcaccc aattataaac 112740 aaaaacatcg cagttaaatt gtttgcagca aacataacca cacaagtttt ttaacacaaa 112800 tgcggtaggt aaccattgtt gccaggcgtg ccatgtgtta agtgttttta aattacattg 112860 tgcgtttaat acaccgagca gtaatctcgg gaggacggtt aacgagcgat atacatattc 112920 cctaaacacg ggaacgcgcg ctgaccaccc tccccaaatc acaacacggg catgtgtaca 112980 aaacctaaat tgttaatgct aattaagaaa aaaacaaaaa accgttagtt gtgcgcaaaa 113040 acttgcaaat gtacccaagg ctttcccctc aactttaaaa cagcggtaat ttgtttaaac 113100 atactaagta aacacgtaga cacccgcatg taaaactata taattgtttc cgttcattaa 113160 actggaaata taaaggcttt gcgtgaaaat ctgctaacgc aaagggcact taatttttcc 113220 catgcaaact tagaaatcta cagctaacgt taataacagc aactttaggc agcaaaacag 113280 tgtccgttgc agaccctgtt agaactcaaa actctatagc aaatgttaaa cggcgactgt 113340 aagcagcgaa tcagtgtccg tcgcagaccc tgttaaatat aaacacaaca gggagcacga 113400 ctaaacacag actaactgct cattgagccc tgttgaagaa ctggcgttgc aatgcattag 113460 ggaatctaaa aacgaaatcc tgctcggtaa cacggaaatt gtctttagtt ccctacagca 113520 ttacaacaat ttcaacctat aaacgtacgc gcgtagggtc agtgtggtgt gtagtgcttg 113580 gtgcaactgt tacacaaggg ggcttgtaaa tgtggtgctt agtgcaacgt gcaggtcccc 113640 cggtggggtg caggtccccc ggtggggtgc aggtcccccg gtggggtgca ggtcccccgg 113700 tggggtgcag gtcccccggt ggggtgcagg tcccccggtg gggtgcaggt cccccggtgg 113760 ggtgcaggtc ccccggtggg gtgcaggtcc cccggtgggg tgcaggtccc ccggtggggt 113820 gcaggtcccc cggtggggtg caggtccccc ggtggggtgc aggtcccccg gtggggtgca 113880 ggtcccccgg tggggtgcag gtcccccggt ggggtgcagg tcccccggtg gggtgcaggt 113940 cccccggtgg ggtgcaggtc ccccggtggg gtgcaggtcc cccggtgggg tgcaggtccc 114000 ccggtggggt gcaggtcccc cggtggggtg caggtccccc ggtggggtgc aggtcccccg 114060 gtggggtgca ggtcccccgg tggggtgcag gtcccccggt ggggtgcagg tcccccggtg 114120 gggtgcaggt cccccggtgg ggtgcaggtc ccccggtggg gtgcaggtcc cccggtgggg 114180 tgcaggtccc ccggtggggt gcaggtcccc cggtggggtg caggtccccc ggtggggctc 114240 cgggtggctc cgggtggggt ggcggctccg ggtggctccg ggtggggtgg cggctccggg 114300 tggctccggg tggggtggcg gctccgggtg gctccgggtg ggcacaggtt ctaaaagcta 114360 cagtaaatcc aacggcaaat ccaacgcaaa aaagtccgtg cgccagccgc gcagaagcgc 114420 gactgcttac ctgtgcttcc ggcgcccttt atataggcca aaacaccctc ccaaaatgag 114480 taacatagtg ttattatgca accataatac taataaatga atcatcaatt tttggttagc 114540 gcaccagcgt ccaaccgccc gccaaccgtg cagcgccgta tattcgaata tcgcgctaca 114600 cgaatacggg acgcggcatg gtagcgggag cttggcattg cgcaataccc aggtacagcg 114660 cgcaggtaca ttgggcccag ctaacgggga ttccccaaac aaggtaaagc ccacatgctt 114720 gctatgtgaa cggtctattc ggggattccc catacctcag acccgccgag agaatattca 114780 gcgggactgt aggctgggtc ctcccaggat agaggtaggg agttcccctt taattaatta 114840 tttatatatt taaaaattta ggctggcata ctataatgga gaaccaggct gggaaccttt 114900 gtaccgggga ttcccctaac aaggtataac taatgtaaac ccatataaat tgattttttt 114960 ttgggaaatc cccgcttgct tttacattaa tatagaatta caggctgtag cattagtaat 115020 ggagaactag gctggagacc taggtaccgg ggatccccct aacaagatgt aattaatata 115080 aacctatata atttcaccct gttaggggaa tccccgtttg tacctgtatt aatataggat 115140 tacagcctgt agattcggta atggatacca ggctggagaa ccaggctgag tgatttacta 115200 acatgggatt caattaacag ggaaaaaata taatagaata tatataatat aggggaactt 115260 gtaaacaaaa cccaactcgc ggattggctg tttgtttggg ccaattggct gcgagaattc 115320 cgtgattgac aggcggttgg gccaatggcc tgcgagcatt tttgattgac agatcgccta 115380 gccaatcgcg gctgggaact cggcagcgaa gcaagaagcc gacggttgcg acaaccaatc 115440 gccgccgcgc gtcggtttga ttgacggctc ggcgggccaa tgggaaacgt ccctgccggc 115500 ggcccttaat cccccggctt aagggattac ggccgtaaac atcgctggcg cggtgccaca 115560 gccgtcgagc cccgcgcccg gctcggtgtg acctccccgc gaccccgccg ccctcatgcg 115620 caccatgggt acaatgggta ccgtgggcaa cattttgcgc tgaccgccgg atgaccccgg 115680 cgccaaagag cggccgatgg gtacgcgcgg cgaccattaa aacatgtttc ggtgaccccc 115740 gcctgacccc gcgccccaaa ttgcgggcac atggtggcgc cggcgcccca ccgagcccat 115800 ttcccacggc ccgcttatgg gcaccaaata ggcccatggt gatatgtttc tgtgaccctc 115860 gggtgacccg gagcgacatt ttgcgctcca tggtcctgaa ttcgccccat gagtacatgt 115920 ttcggtgacc cgccggcgac cccgggcggc aaaaaccgcc ccgtgggcac caaacggcac 115980 catgggcaca tcttttcgtg acccgcgggt gacccggcga tggcaccgcg ggcgcggggg 116040 gtgatatgtt ctgatgaccg ccgccttacg ttcgcagcgg tgtcagcgga acatattctc 116100 ccctgctccc gggctcggga cccgcggacc cgagtcgagt tattaaagcg acattaggga 116160 ttaattttaa tccccgaccc cctttaatgg tgcggctagg ccggctgcga cgttgacgcc 116220 ggcgggttcg acccattgac cgcatcctcg gtggccgggc agaggccggc cggccaaagg 116280 tgcgatcgcg gggtctaacc cacccgtgtg agagagccct ccgttgcgtt gtcttcggcg 116340 ttcctgaccc cctggctcac cggggatgtc ttgtgagcac tttcccccgg gttacaatgg 116400 acaggaaagt gctggcaaga catcgacggg gttgccggtc ggggaacggg aggcgcgccg 116460 gtacgccgct tgcgtgagtg aggtggcgcc gatgggccgt atgacgaccc ccgcaacgcg 116520 aagggccgct ggcgcggaca tttcccagaa ccggccgcgc cgccaagcgg cgcggctgcc 116580 tcccccaacg acccttattt tagcttttaa gttgttattt aaagctcggc tgtttgtggc 116640 acgcgcttaa gcgttgccac ctgctgcgga gatcccccgt gcgcatcgcc gccctcctcg 116700 cctcagtgca cgctgccgag cgtgccacct gtttggttgt catcccatgt gcgcatcccc 116760 ccattttgtc ttcccgaccc ggcaacataa acgtcacgtt gtttgtgaaa aataattgtt 116820 tttttttatt tttgttaacc cctcaacctc aatacagtct ctcgccttcc acccgttgtt 116880 ttgttaccag cccccctctt ggcgaccggc accggcgtta accgggtgcg ttggcggcca 116940 caaccttggc cacgtcgcgt ctggagacgg cctgcagcag gtcttttaaa accaggtagt 117000 ctgaggggct gaccagggca gccttttcca tttgcgagat ccattgaaaa aaggtgggtg 117060 actggttgcg tttgcgaccc agctggttgc ccgttaaaaa aactaaattt tttacgtccc 117120 tttctgagag ctgacggtta atggagagca ttaggtgttt gtacggacta aagtaactgg 117180 ggctggaccg gagcctctcg acaataaatc ctacgtctag taaaaaaaag gtggagacca 117240 ggtccaatcg cccgacgaga aacaccgcct ccagtaacac cggaaaggga ataccgggtt 117300 cccctgttgg ggggcacagc ccgtttgcga acccctcggg tgtattgtcg gacaccggcc 117360 ggtcaaaaag ccacagcacg gcctctctgt cgtctgcctc taggtggcga ccaaggtcca 117420 ctatccgctt atgcgggaac atgggtccgg tgcggcgctt gccaacaccc tcttttacct 117480 acgctggagc gtttgagaaa tcacgacgaa ccgcgggcgt tatttaaaat gcggtcttcg 117540 tctaattccc gcaaggtggt ggcaaccgac tcggccgcgg ccgtgagggt tgcggccgaa 117600 acgccgatgg cctccgccaa tttgtccaga ggcggcgcag cggcgccgag gctaaacagc 117660 gcgcaggcgg ccgccaccag ggacggggaa agcccgccgg tgaccgggtt cacgatggct 117720 ttgtgaacag actccaccac ccggctgtga agggcaaaga gctgctcttt tgtaaagccg 117780 cttttaaaca aggcgggccc gatggcgtcc gttggtaaaa ctgcttctag tttccacctt 117840 aaagccttaa ggaccgattt ttcctgtttc agtaaatccg ccacggaaaa atcatccgcc 117900 gcgcaaaagc acaaaaaggc ggccttaaaa ggattcaggt ctctaatctt gccggctaaa 117960 aataggcagg cggcccccag cctttgaaac cgccgacggg ggatgctgcg acactctaga 118020 tagcgatcca gaatgctgac ggccagggga aaaacgctag catccgcctg gtgggccctg 118080 gcaacagaac gcatccacgt ccccaagata actcgcatgc ccaaagtcac ctccgtttgt 118140 actgtcccgt agcaggccgt ggatgttaca aaggacgttt cgtgggccag gaggttagaa 118200 agggcccggt cctggtacag gacggggtca atggtcccgg tgggcactgg gccaacaaaa 118260 gccattatta cggcaaggta aagaaagcga gataagtcct acctgcggct cacggaggct 118320 taataccaac gaccggctta acacccgatc ttctttgcgc tctatgtccg ctccacagca 118380 atcccatgtc ttgtgcagtt cagccctgcc tgttcccgga aagcggcgga ctagagtcaa 118440 cgcggaagcg gctgttcatt taaggtgagt cacaggcggg gcaatttgcc agccagtgac 118500 gcgtttcctg cagtctgggt ttttacctgg caagcgccac tgatacttgg cagcctgccg 118560 gtggggattt ttttagtgct gaattggcag tcctctgtcc atgcgcacta tgctagcatg 118620 gaagtggggg gcggatgggt gaaattgttc ccaccggcga cgggcttttt tgacggcctt 118680 ggcggttccg cgactttgac agaacaccgt gatgcaaaaa gccgggatga cgggacttcc 118740 aggtgcgtcc ggcaaaacgc ggacgctgga tgctctaatc ccgggaaact gtaggcacct 118800 tgccaggcga tacagtgaat aggggtctgg gttacaaaag atgactccgt gacaccacgg 118860 gcccggtcga ggggggtcga ccctgtctcc caacgcctga cgataaaatc ttctttgtgg 118920 gcggtatttt cttggtatct cctcctcgga tgagggtacg gtatgggaat ggggtatcgc 118980 ggcgggcgcg gggggcgcgc cggttgctgt tgccgctcct ccccctcttg ctcccgttgt 119040 ctttcaggaa cctcgtcctc gtgggagttg tgactcgtgc atctgagacg taaacaagga 119100 actcctccgg gacgcctggg tggaccccaa ccccccacgg tgtacgtgtg ggatgtatgg 119160 ccaggaaacg ggggtcctgg ccgagacggc ccggcggggt ggtctgtgtg gctcaccgcc 119220 tgttgcgtgt taggggatgg ggcctgttga ggcgttggcg attgctgtgg tccaggtgag 119280 tcgggcgggg attgcggagg gggcgaggac gttggcgttg gcgattgtgg tggtccaggt 119340 gagttgggag ggggcgagga cgttggaggc ccaggcggtt caggtgagtc gtggggcaac 119400 ggttgcaaaa acgacggagg ctgcggatcg ggcgatggat gatgcgacga cggcggtgca 119460 ggtgagaggg gggcggggtg cgatgggggt gatggtgggg gcgaatgcga tgcgggggat 119520 cccggggacg accctgatgt gtttcgaggt gacaggtctg aagctaacac cggcgcagac 119580 ccgcttggcg atggcgttgg agatcccaac acgatgacgg actcagaccc cgaccccgaa 119640 ggcgacccct gtgatgaccc gtgcccggac tcggtggccg tttcggtgtc cgatccgtgc 119700 ccttgttcga caaccaccag aacctgtggc ccaggcggcg ttggggaagc ggaggccgcg 119760 gatgcggagg ctggtgcggc cgcgccacgc cccctaccgc gactgcgccc cccggcctgt 119820 tctctagtgc cgccgcgtct tccgcaatgt cccctgcagg aacttcgcaa cccgtgtccc 119880 gatactatgc cggaacgatg ttgccggctg ccccacatga tcgcggttta ctgcgtgtaa 119940 aaaacgacag attaagtaga ttgccctttc cacgacccgc agccacctga gcgcgcgcac 120000 gcagaaccta tgtttagtgc gcttgcgatt atgtccgcta ggtggcgggc tattttgatc 120060 aggccgcgca cgcattgacc gttaggtggc gcagagcgcc gtaaaccgca gagagcaccg 120120 cacggcggtt ttagtttcgc tactataacg tttagttaaa atctgtggcc gatattgggt 120180 ggcagtatgt aattcacgcg cgccgcggcc cccttacctt gttgccggcg aaccgcggaa 120240 actccgttcc gccgcgcagc gcgcggccgc tgccgaaacc aacgccgctt gaatttcgcg 120300 ggcggccggg cttggtgtca atgattcaca cagatgcgat gtgattgggc gtggtggtta 120360 acgtcacttg ttaacccgta aatctggaaa ttcttgtccg ccgcggcggt gagccgcggc 120420 cctaagcctt atagtgctgt gcagcgatcc tgaaactcga aagctggcca tataaacccc 120480 agtatggcgt tgcgtgtcgg tggcaacctt tttgaaaaag atttattgcc gccaggtgtt 120540 aagcaccggc accgaccgtg cgttttcaat catgttggga ggaattacat taacgctgct 120600 gctggcgacg ctcgccacgg ttcggtgcgc tcttcaaacg cactatgcgg cggtccccgt 120660 gcactctacc gcgtcccttg ggtgcgtgtt aacaacagcc cacaacgttc ttatcgttac 120720 ctggcaaaaa caggaatcgc ctagccccgt taacgtggcc acatatagtt ccgaagcggg 120780 cacggtggtt cagcccccgt tcgccggtag ggttgacatc cccgaacaca agttgaccag 120840 aacaaccctg aagtttttta atgccactat ggaggacgag gggtgctacc tgtgtatctt 120900 taacgcgttt ggagtgggaa agctgtcggg aaccgcctgc ttgacggttt acgtccccct 120960 gtccatgtcc gtcacgtttt accccccaat taacccgacg caacttgtct gtcgggccga 121020 ggccagtccc gcaccgtctg ttaactggac cggcgtgcca cccgagctgt gcagcgaacc 121080 cgaagtgttt ccccgaccca acggaacaac cctggtcgtg ggtcgctgca acgtaacgtc 121140 ggtggatccc gaagacctca gaaacgccac gtgcctggtc actcatatag gaggtttggc 121200 ctcggcgcgg cccctgggcc ccgtgttttc ggatcctctg gaagggacga gccactacgt 121260 ggtgggtgtg gtggcagcgg tcgccgtttt aggcattttt ttaacgggtg tttttttgta 121320 taggtctatg tgagcgcgcg tggcccccgt gtctagtgtt ttgttcccca gtgagtgtct 121380 ccatgacaaa tacaaatttg aggctggctt ttagggtggt ttctcgtgca acgcttcctg 121440 tgtgactgca tacaccgggg tgtcaccagg aaaccgcgtc tcccctttat gttcgctcgc 121500 cctctctgag cgaaggtgag aatggtaccc ggggcgtttt ggcgttgaga gagtcgggcg 121560 atgttgccgt ggcggcgtct gcaaaggctc acccgctttt gttttttccc ttttgccaga 121620 caccgacatg gacgccttga acaataacct taacctgctg atggattttc tttcaaacta 121680 ttcgaatagc tacagcagtt atgacgataa tatatcttac accttagaca cggaatccac 121740 gctgtgtcgg ctgactataa ttttcccacc tactatttat gcgattatat gcttttttat 121800 tttttgcatt acgctgctgg ggaacgcttt ggtgctatat atatttttta aatttaaagc 121860 tctcgccaac tctgtggacg tgctaatggc ggggttgtgt tgtaactccc tatttctgtg 121920 cgcgtcgttt ttgttcagct ggctgctgta cgtggcgccg cagattctca cgcccgcaac 121980 gtgcaaggtg gaaatctttt tcttttacct gtacacttac tttggcgtgt acattgtggt 122040 gtgtattagc ctcatcaggt gcctgttagt tgtgttttcc cgccgcccgt gggtcaagca 122100 ctgggcctcc ggctttctct gcgtgtgtgt gtccttaatt gtggcgctgg cgctgtctgc 122160 caacgcgagc ctctatagaa cggccctgcg ccacccagag accagcgagt ggatatgcta 122220 cgaagatgcc ggtgaagaca ccgtcaactg gaagctgaga atcagaacca tcagcgcgat 122280 ttgcgggttt ttggttccgt ttgggctgtt ggtgctgttt tatggactta cgtggtgtat 122340 agttaaaagc acgaagctgg ccagaaaggg agccgtgagg ggtgtaattg tgacggtggt 122400 ggtgctgttt ttaatttttt gccttcccta tcacctgtgc aatttttttg ataccctgtt 122460 gaggaccggt ttcgtgaccg aaacgtgcta catcagggac gtaatcagcg tggccatgca 122520 catatgctct ctgctacaga gcatgtacag cgcgtttgtg cccgttgtgt attctggtct 122580 tgggtctctg tttaggcgaa gggttaggga tacctggtcc atgtttaggt gtttttccac 122640 ctcgggtagt ttatgagaca ctcaaaagac acttggtggg attgtttgtg tacatttatt 122700 ttttattttg tgtacatttg ttttcattaa agcgatctga cctgcagacc ttacctgacg 122760 tttactgcct gtttcttacg caccagagga acagggactg gaaggccagc gcccacgggg 122820 aaattgtcat gtctgcgagt tcgggcggca cgtacgccca ctgccagggg tggaacacca 122880 cggctgggtc taccagcgag gccaggtggc gcccgtccgg tgacgtgatg gcggccacgg 122940 ccgagttggc agacgggttg cgtgggtagt gctgcgcgaa cattcttggg tcggggttgc 123000 cagtgtggaa gttcagggcg atgcgctgct gctggttcag gtggtactca atggcatcgc 123060 gcgggtatct cacgcccagg taccggccgt tggcccaccc ggggaggacg aggccccgaa 123120 ggaccctaaa cattatgctg atggtggtct gggggatgtg gaggtttagc cagaggcact 123180 cgtggttccc tgatgcgttc tcctccaggt ggatgtccca ctggtcgggg gttttgggcc 123240 cgggcgtgtc gtgaggggtt tctctgagta gaccgagcgc ccccaggagc tggaacccaa 123300 actccccgca gcacagtgaa aatgtatccg ctcggcggaa gaatgccata aggcccccat 123360 agcacccagg gtcgttgaga agacccatga ttgcgcatcg ggcccccacg tagctgtctt 123420 cgatgcccac gtttccaccg atggttaagc cggagaatcc ccggaggatg ttccctcctc 123480 taaggtcgtt ggtggagacg gccgcgacgt cgaacccgac gttagtgaat gcggccatca 123540 gcgccctggg gagcggggcg ccgggggcga tcagggcggc cacggccggt ggcctcgacg 123600 gcaccgcaaa tagcgtcagt tcgctgtttc tgcagacgtc ggcgaggtgg cccaggttgt 123660 gtcggttgca cccgtagtcc tttctgtaga gttcctgcgc gggcgtgaag ctgggccccc 123720 aggagtacca ctgttcgtcc gagaacgagg tccagttagc ggccaccgaa gtgagggtct 123780 gggagtaaac ttcctcgttg ttgtgtgaga tgacgattct ttccgacaga ccctcctggc 123840 ccacggtgcc gcacactgtg gcctggcagt caaagttctg gcacgcctgg cgcacctcgt 123900 caacgtgctg gggcaggatt tcaaaaataa cgcccggggt ttcggacacc agccacggca 123960 ggggcgtttc ctctgacgga atgcaaatct gcaggcctcg gttaccggcc agggccatct 124020 caatagcggt gaccactacg ccgccgtcgc tgacgtcgtg gccggacacc accagacccc 124080 gggagagcat agactctgtt agcataaaga ggttggccag gtgtgtcgcc tgaacgtccg 124140 gtagggtggg actcggcaga agacacaggt gctcgaaggt tgatccctgg gtcaggtgcg 124200 gtccggggaa ggttactagc acgaggaggt tacccgtggc cttgaggtca ggtgtgacgc 124260 gtcgcctgga cgactttacc tcggcggtgg ccgtaatgat aaccgcgtta aacggcacgg 124320 gggccaccgt ctgatgctgt tgcgtggcgc tgatcagttc ttccgacagg cacggggtgc 124380 tgccggccga cgtgatggca aagtttacgc tcaggtcccg gcatagttcc ttgcaggcaa 124440 acagtgcgtg ttgcagtagc caggcttggt cttcctccgg gttccaaccg acagacgccg 124500 tcagcgtaat gtcactcagg cgccgcacgt gcgctagcat gatgttggtg accgcctcgc 124560 agatggcgta tcttgcgccc actgccgcgt cgatgcccat cttgtacgcc tgttctccgt 124620 gggccacgca ttgtccgacc cacctgagtc tgcccctgcc ctgggtgacc caggtttccg 124680 ggctacccag gcgttccgtc gcgtcctgcc tggtgatcgg ttgggggcga tgtatgggca 124740 cccgcgccat tctgtccgta aacaccgccg tgtggttgac gatgtggtaa tctgacagcg 124800 gtcggcccag gggtcccact tcgcactgct gagctacgag tccgttggag catctgtcca 124860 catgtcgcgt gacaaactct ttgctgccga cggttggaca tcgcagaagc tgatcgacca 124920 cggaggccag gcggaatagg ccccagtctg tcggcgaggg tgcctgttcg ccgccctcct 124980 ccggttcttc tgggcgcacc agccagttgg aggaaacggg ctgctcgtcg aacccaaaag 125040 ttgcgatcac ttcggccgag gtcggctgtc tgatcggcca cgctcccggg ttccacagct 125100 ctaggtcgtt cacgaactgg attcccggct cttcgcaggt ttccccgacg acggcaaaag 125160 ggcatccaca gatgcgtgcg gcccttctga tggcatccaa cgggcccggt tccggctccg 125220 tgtcgcgcgg gagaacggca aagaccacaa aggccgacac gttgagaaac ttgttaagta 125280 ggatgtcgtt tacggtttcc cgtgagatgt ctggcgtggc ggtcagttgg cttagaatgg 125340 tcggtggaag ctgagagacg aagaggcgaa ggccgccccg cgagaccagg gctcccaggt 125400 ggctgatggt agaggcgggt tcgtgggcgc gattaatgct ggtaaagagg ggcccttcca 125460 aaatctcgta agccagcgac aacgtttggt taatgcgatt aatacctgcg gcgctcccca 125520 ggtaaagaga gcgctggttg ccatcgccgt caaccggttc aaaagaccca agacagatga 125580 taggctgatt gaataaagac ctcctgagga atgtgtatgc ttgaggcacg cacgataaca 125640 gcgatgtggt ggtaataacg ttcgcctcac tggtggtggc gctgtggacg gttttaagaa 125700 agccaccaag gacaggcgtg ccggtgcgcg ccagctgctg gcagtggagt gtcgttgttg 125760 tgttaatagc tctgtggcgt gcgcgagaaa atgcgcccac tgacggcgta gtggcgtaaa 125820 atccacacag ggccgatcta atgtcgcccc cgggaagcag cgtggaatgg aacaggatgt 125880 cctgcagcgc acctgcacct gtccgaatgg cgctgtgcag gtgtgtgaat gagtcagcta 125940 tgtgggttac gttttcgcac ggaaggcgct ggaaaacgca gccgtagctc ctgcgggcca 126000 tgacggcgta tctggacacc gtatagctgt tgccattgga ggcctgtacg gccaacggta 126060 atatgttccg ttgtaacggg agcatcaccg cggcgcatat tgggtctctc tccggcaacg 126120 gtctccaggc ggtggattgc actgtaaccg ggagctggcg ctgcacgcgc acatcatatt 126180 ctactagtgc gccaagtgtc agggcggcaa atgtgcccgg gggtacccgg tcggcgacaa 126240 accgtctagt ctggcagctc agatgtctgg ccagttctaa ccgcaacgct gtatcaaagc 126300 cgctgtctct aaggcactgc actagttcgc tagatcttgt ggtaggttgg cgcagtaggt 126360 ctgggccata gggtagggat atagtatgat ggccctgaag gtgcgccgac cgagtttcca 126420 gaggtgcata attaaccaag ggcgccagga gctgccagat aacgcccagc gttgggtcgt 126480 catcgtcgtt gtcaaagtta tcagaggggc gggttacaag ccaaagtaaa aattcactaa 126540 agcactgttc tggcacgagc gccaaaacgc tttctgcatc agaattgtca tgaataaaag 126600 cctcctcgtc tgcactaagg gccgcggcgg cccagcgagg gttcgtgcgt tgggccatgt 126660 ttgctaagtc tagccggtgc aaaagcaagc gtatgggact ttaatagggc gtgtaagggt 126720 tgttaggtat ttggggggta tttgtttatg ttagatgaag tacaaaccta tgttatgtta 126780 gttttggcca ccttcacaca ctgcatcaaa aaactcccca atgttacagt aatcacttga 126840 caattcgccc tccaactcat agaagctatt ttggggagtt gaagatacag gtaagggggg 126900 gaggggaatg ttaggtggcg agaggcatga cgctgaaggg gaggggctgg gaataacttg 126960 gaggggttga cttacgctta ttggatgatc aacggttatt tctgaaagtg ctacccgctg 127020 gacggtaggt cgtgggttag gtaaaacaga aagcggtagg gaaattgacc tcagggccgc 127080 ccctccgctg gcgcgttgcc ttttaacatc tagtgctgta tggatgagcg gttcatcgcc 127140 tgccccggag tttgtgggcg tggtccgagg gaggatgttc aagtcaatgt taacttcctc 127200 ttgagaccgt ggacgggccc gtctgtagtg tcttgtggag ggggttgtct caacgtgtgt 127260 tggtgtaaac aatccaggta atcggtaaag gcacgcggtt agtccaattt gcagaaaacc 127320 taaaaacaca aaataggctc aaaaaagtac ttttgtggcg gttaataaaa ttccggcgcc 127380 aacgtctaca caaagcgaaa ctactcacca attagtaaaa tgccaactga aagggtgata 127440 acacttagag cttctgttcc gatcggttcg aatttcagaa tggatagcaa atttgccccg 127500 ctgccaatgc ctggaaataa gcggtgtgta ttttacatgt ggtacaggac aaaaaacctt 127560 gtaggtttca gttgagtcac cctgccacgt aaacccgcct agagtgcggc acgcgttgtc 127620 ggttgcagga agtacatact aattttaact tgaaaaggtt tattgtagaa ttgtggtcaa 127680 aattatatta tacttacata acatccaatg aacatttgca ctccagaatg atattcggtt 127740 taatgcgtga taaaataagt ttgcaacaaa tgcagcgacg agtaggccca ggaatataaa 127800 aaacactgca taaaagataa tgttagttag tgtttgtgtc acataaatgt tttaaaataa 127860 cagtgtgttt tgtgatgtta ccgagtttgc tttctggcaa tttagtgtga ataatatgca 127920 ctccaatttc tgcggcaaca acgtgtagtg caagtacaat tccttgtagc ataataaaca 127980 agcaggttcc atgatttgtg cttctccagg ccttcttaca agcaatatac attgcaacaa 128040 cagctgttaa aaataacaca attaatataa taaactaaca ttaatatttg gaatttacat 128100 tattaaaaca aaaagacagt attaaaaaat accagtgttt gctgtaataa tagagtatgc 128160 taatgccatt gttaaagatg atgtagtact tgcttcagtt actgcgtaca tgccaatgag 128220 agctgtaaca aaaaataaac agttaatttc ttcataaata ttgcctctgt ttattataaa 128280 taacaacaaa attgcaacat acctgcatat attgcaaacc acgatccaat tattcttaca 128340 atgtttgttt gtgaacttaa ccatacatat ccataaaatg ccattgctat aaatattggc 128400 ggtattaagg gtataatttt gtagtgtcca ttccataatg ttattgttat aaaaatcata 128460 agtattgccc atagtggcaa aactaacaaa catggagtac ttgttaaaga acagcgaggt 128520 gtttgaatag caaaaagaaa agtgcctgta aaataaacac acaatgctgt tagtaaaaat 128580 aataaaaggt atttcaacaa aatgtgtttt ataaataaaa tttcttacct atataaattt 128640 gggatacaaa ggcaatagca atacacgctt tcacaagtaa agttgaccca tgtaacgaaa 128700 acccggacaa caaaacacag caagctagaa aaacaaatta tgtaagtatt agtggttatt 128760 atgtaataaa agaccgcttt ccgccaaatt ataatgtcat acctgtaatc cacggtatta 128820 gcttcaataa aggtgtgttt aaccgttgtg atctactctg ataaaaatac aatccaagag 128880 atttccatag gaaaaaaaaa caagcaactg tagacacagc aactatataa aggtctttgt 128940 tattgtcaca ggcatattgt gccagtgaaa taagccaaaa tgttcctgtt aaaatgtttg 129000 aaaataacca ggtacaccac acaaaaaagg ggcagttaca cgccatgttt aaaaaatcag 129060 taaaaaagtc tacacaagtt aaagggggac tttagtttaa acgccttatt acatcgtttc 129120 caggcagact tctcactgag tcacacaaag gtttctatgt tcccctgtcg ggaatttgcc 129180 ctagtgctga tttcgttggc aaacaaccat ggaaaagcga actgggaata tttgtttttg 129240 ttagctggcc ttggatgctt gcaaacattc ttgttattct aatgttaggc caaattgtgg 129300 gaagcattaa gaattgttat tgaaaataat tctatttaat caaaccatgt ttcaggtccc 129360 agaagggttg tagtaatgtg taataggaaa caggcctaat acagaacatt ctgttgggta 129420 catgaactaa aaatatgttt aatgagggct gaggtaaaag ctagggtgag ggctggggtg 129480 agctagggtg agggctgggg tgagctaggg tgagggctgg ggtgagctag ggtgagggct 129540 ggggtgagct agggtgaggg ctggggtgag ctagggtgag ggctggggtg agctagggtg 129600 agggctaggg taatggatac gtttaaaata ttaggctacg tttttactgt tatgtaattt 129660 gcgttactgt taccttgaat gtgaattagg catagggtta tagtttataa accacacata 129720 tgtaaagtaa ataaaaaata aaatgcgaac caagctggca caagtaactg cacgctaccc 129780 taaacgtaca atactgggac tagaacccag aggtagttag agtatacggt agttacagaa 129840 ctttacagtt cctttaggcc agcagggctc tgtggttaat taaacaaagc ttaaagataa 129900 ctgaaaattt aggaagtgcg tatgagtgca atgtgttcca aatcgggcaa gggttacata 129960 aattgttgcc tagcagcggc gccaggcgag ggcccctagc ggcggcgccc ggcgggggcc 130020 cccaggcgcc cggccggcgg cggcgcgggg ccgcggccgc catcttgcgc ccggggcgag 130080 ggtctcccgc gcggcccccg ggcccccgag cggggcgccg ccggcctccc ccggctcccg 130140 gccctccgcc cggccggccc gggcccgcgg ccgccgcccc cggccgcccc gcgccgcgcg 130200 ccgggccgct ttcggttcgc ggggccgggg gtcccgcggg gggccggggc cgcccccggg 130260 tcccgctccg ccgggccccg ccgactcccg ggagcgcccc ggtccggccg agcccggcgg 130320 cgccgcgccc cgacgccccc cgagcccggg gccccacaag ccgcggcgcg cggctcccga 130380 tgccgggcgg ccgccgcccg gcatggcggt cctccgccgg cctcccctcc cccacgtcgc 130440 cccgaaaggt ggtctccgcg ccgccgggag gggggctggg gcccggggcg cctcggcggg 130500 gccggccccg gggcgcgacc gagggccccg ggagaacggg ggatcgggaa aacgcgaggg 130560 gtggcggggg acagagggga acgtgtgcgt gcttgtggaa cactatggcc tgctggcctg 130620 ctcgcttgct tggtagcttg caagcttgct gctgagggtc tttagaggga cagtaggcct 130680 gcttgctggc ctgcttgctg gcctgcttgc tggcctgctt gctggcctgc ttgctggcct 130740 gcttgctggc ctgcttgctg gcctgcttgc tggcctgctt gctggcctgc ttgctggcct 130800 gcttgctggc ctgcttgctg gcctgcttgc tggcctgctt gctggcctgc ttgctggcct 130860 gcttgctggc ctgcttgctg gcctgcttgc tggcctgctt gctggcctgc ttgctggcct 130920 gcttgctggc ctgcttgctg gcctgcttgc tggcctgctt gctggcctgc ttgctggcct 130980 gcttgcttgc tgctgagggg acagtagggc tgcctgcttg cttgctgctg aggggacagt 131040 agggctgcct gcttgcttgc tgctgagggg acagtagggc tgcctgcttg cttgctgctg 131100 agtaggactg ctagggctgg agtagggggc agccggccag ctgcgtgcga gggcgttgca 131160 gggtccacac gaggacacgg gacccgagcc ctccccagga ccgccgggca agcggcc 131217 2 98 PRT Japanese Macaque Herpesvirus 2 Met Arg Trp Ala Trp Phe Ser Pro Phe Leu Ser His Gln Leu Gly Val 1 5 10 15 Ser Asn His Ala Pro Ser Pro Gly Pro Thr Ser Ala Pro Leu Pro Ile 20 25 30 Pro Leu Leu Pro Val Pro Ser Pro Ala Ser Met Leu Pro Ala Pro Thr 35 40 45 Ala Leu Ser Val Arg Ser Pro Arg Ala Thr Cys Arg Ala Asp Leu Gly 50 55 60 Arg Leu Pro Gly Gly Pro Gly Glu Gly Ser Gly Pro Val Ser Ser Cys 65 70 75 80 Gly Pro Ala Thr Pro Ser His Ala Ala Gly Arg Leu Pro His Tyr Tyr 85 90 95 Gln Pro 3 425 PRT Japanese Macaque Herpesvirus 3 Met Phe Val Leu Leu Ile Phe Ile Leu Leu Gln Pro Ala Ser Leu Glu 1 5 10 15 Leu Leu Pro Ala Lys Leu Thr Ala Val Pro Thr Trp Cys Pro Pro His 20 25 30 Pro Gly Asp Thr Tyr Leu Leu Thr Cys Arg Gly Thr Ser Thr Ala Arg 35 40 45 Asp Gln Arg Ser Thr Gln Trp Phe Arg Asn Asn Thr Leu Met His Gly 50 55 60 Ser Asn Phe Tyr Gly Arg Leu Val Ser Val Thr Pro Asn Ser Thr Ile 65 70 75 80 Ser Asp Trp Tyr Ala Cys Gln Thr Lys Thr Thr Thr Arg Ser Asn Ser 85 90 95 Ile Asp Phe Arg Val Arg Ser Ser Arg Leu Thr Leu Gln Glu Arg Cys 100 105 110 Ser Ser Tyr Gly Tyr Ser Asn Ala Asn Asn Thr Arg Val Leu Arg Cys 115 120 125 Tyr Ser Gly Gly Asn Val Thr Leu Arg Asn Val Val Phe His Leu Asn 130 135 140 Gly Thr Ala Val Ile Asn Gly Thr Thr Thr Asp Ile Tyr Thr Phe Val 145 150 155 160 Leu Thr Glu Lys Thr Gly Gly Thr Tyr Tyr Cys Ser Ala Phe Ile Gly 165 170 175 Thr Glu Lys Leu Tyr Ser Gln Lys Ile Asn Val Phe Phe Thr Ser Phe 180 185 190 Thr Phe Lys His Thr Asp Asn Val Gln Asn Gly Ser Glu Phe Asn Lys 195 200 205 Thr Glu Gln Ile Gln Gln Thr Ala Asn Val Gln His Thr Ala Asn Tyr 210 215 220 Val Val Phe Ser Val Pro Val Phe Ser Ile Gly Val Leu Thr Gly Ile 225 230 235 240 Ala Ile Ser Leu Ile Met Cys Trp Leu Phe Thr Leu Arg Cys Asn Lys 245 250 255 Asn Ser Glu Ser Ser Asn Asn Arg His Ala His Gln Thr Ser Tyr Ile 260 265 270 Gln Pro Ser His Asn Gln His Ser His Thr Ser Glu Ser Thr Thr His 275 280 285 Thr Tyr Arg Asn Asp His Gln Glu Glu Ser Ile Glu Glu Leu Pro Asn 290 295 300 Gln His Thr Arg Lys Thr Asn Ser Cys Gln Thr Val Leu Leu Glu Val 305 310 315 320 Lys Asn Val Ala Phe Asp Gly Pro Gln Gly Asn Leu His Asn Thr Asn 325 330 335 Asp Glu Val Met Glu Gln Tyr Asp Asp Val Val Val Glu Asn Ile Glu 340 345 350 Gln Thr Ser Tyr Asp Asn Asn Ile Glu Gln Met Asp Tyr Ser Asp Ile 355 360 365 Ile Arg Pro Asn Phe Asn Tyr Tyr Ser Gly Leu Ile Leu Glu Glu Val 370 375 380 Asp Glu Val Phe Tyr Asn Glu Leu Ala Asn Gln Tyr His Gly Leu Ile 385 390 395 400 Leu Glu Asn Leu Asp His Asp Glu Tyr Asn His Leu Asn Lys Leu Asn 405 410 415 Met Ile Glu Gln Tyr Asp Trp Leu Glu 420 425 4 193 PRT Japanese Macaque Herpesvirus 4 Met Asp Ile Thr Val Asn Cys Ile Val Ala Val Asp Lys Gln Leu Gly 1 5 10 15 Ile Gly Lys Asn Gly Thr Met Pro Trp Pro Tyr Leu Lys Asn Glu Met 20 25 30 Met Tyr Phe Gln Lys Met Thr Ser Thr Pro Ser Val Ile Gly Glu Lys 35 40 45 Asn Val Val Ile Met Gly Lys Arg Thr Trp Phe Ser Ile Pro Glu Lys 50 55 60 Lys Arg Pro Leu Ala Asn Arg Ile Asn Ile Ile Leu Ser Arg Glu Leu 65 70 75 80 Arg Glu Pro Pro Lys Gly Ala His Phe Leu Ala Arg Thr Leu Asp Asp 85 90 95 Ala Phe Asn Phe Tyr Arg Gln Tyr Lys Leu Thr Lys Gln Leu Asn Thr 100 105 110 Val Trp Val Ile Gly Gly Lys Ser Val Tyr Glu Ser Val Leu Asn Tyr 115 120 125 Glu Cys Ser Leu Lys Leu Tyr Ile Thr Arg Ile Met Glu Ser Phe Asp 130 135 140 Cys Asp Val Phe Phe Pro Ser Ile Asn Phe Thr Glu Tyr Thr Met Leu 145 150 155 160 Ser Glu Leu Pro Gly Lys Asp Thr Asn Phe Glu Glu Asn Gly Ile Lys 165 170 175 Tyr Lys Phe Gln Val Tyr Glu Lys Arg Leu Ile Asn Lys Ala Val Thr 180 185 190 Gln 5 395 PRT Japanese Macaque Herpesvirus 5 Met Arg Leu Ile Met Phe Trp Phe Pro Val Thr Val Cys Phe Val Cys 1 5 10 15 His Phe Ile Leu Val Asn Ala Gln Asn Glu Thr Asn Val Thr Cys Asp 20 25 30 Lys Pro Asn Phe Asp Arg Phe Met Val Ala Met Glu Lys Lys Glu Lys 35 40 45 Tyr Val Leu Gly Asp Lys Val Glu Leu Thr Cys Arg Pro Gly Tyr Thr 50 55 60 Leu Gln Gly Lys Val Tyr Val Gln Cys Leu Gln Ser Gly Met Trp Thr 65 70 75 80 Thr Pro Asn Ala Glu Cys His Arg Lys Lys Cys Thr Asn Tyr Gly Asp 85 90 95 Ile Leu Asn Gly Gln Val Ile Val Pro Asp Ser Asp Asn Ala Phe Lys 100 105 110 Phe Gly Thr Asn Ile Thr Tyr Lys Cys Asn Thr Gly Tyr Leu Leu Leu 115 120 125 Gly Ser Met Val Arg Thr Cys Leu Leu Thr Gly Asn Ser Asn Thr Val 130 135 140 Asn Trp Gln Pro Ala Ala Pro Thr Cys Glu Ile Glu Lys Cys Lys Lys 145 150 155 160 Gln Pro Asp Ile Glu Asn Gly Lys Tyr Tyr Pro Val Gln Asp Phe Tyr 165 170 175 Asn Tyr Leu Glu Thr Ile Thr Phe Thr Cys Asn Lys Asp Phe Ser Leu 180 185 190 Ile Gly Asn Thr Thr Thr Thr Cys Met Thr Asn Gly Thr Trp Ser Ser 195 200 205 Pro Val Pro Lys Cys Glu Gln Ile Thr Cys Ser Ala Pro Asn Ile Glu 210 215 220 His Gly Thr Leu Leu Val Gly Ser Ser Arg Val Tyr Lys His Gly Gln 225 230 235 240 Ser Ile Thr Ile Gly Cys Glu Asn Gly Phe Thr Leu Asn Gly His Lys 245 250 255 Met Cys Thr Cys Glu Tyr Ser Ser Trp Asn Pro Pro Leu Pro Thr Cys 260 265 270 Val Pro Ile Asn Lys Thr Val Pro Thr Pro Ser Glu Val Pro Ser Pro 275 280 285 Gly Thr Asn Lys Gln Glu Arg Pro Thr Pro Glu Asn Pro Lys Ser His 290 295 300 Glu Ser Glu Thr Thr Thr Glu Thr Pro Lys Thr Gly Thr His Lys Ser 305 310 315 320 Glu Thr Pro Ser Lys Lys Ile Pro Asn Pro Glu Thr His Lys Pro Thr 325 330 335 Thr Pro Lys Ser Gly Thr Ser Glu Gln Thr Thr Asn Arg Pro Ser Lys 340 345 350 Ala Pro Ser Gln Asn Pro Pro Met Glu Pro Pro Met Ser Lys Trp Lys 355 360 365 Arg His Val Val Leu Val Leu Phe Ala Ser Val Ala Ser Leu Leu Phe 370 375 380 Val Leu Val Thr Leu Tyr Cys Cys Phe Leu Lys 385 390 395 6 1132 PRT Japanese Macaque Herpesvirus 6 Met Ala Ser Lys Gly Asn Ala Gly Gln Pro Leu Glu Asp Asn Gln Gly 1 5 10 15 Ser Arg Ala Pro Ile Gly Ala Cys Gly Tyr Val Tyr Ala Tyr Ser Lys 20 25 30 Gln Asp Phe Pro Phe Ala Glu Ala Ser Ile Leu Gly Asn Arg Pro Ser 35 40 45 Gly Ser Gly Val Phe Ser Leu Pro Ile Leu Tyr Gly Leu Thr Val Glu 50 55 60 His Glu Phe Pro Leu Thr Val Lys Ala Ala His Lys Lys Val Asp Thr 65 70 75 80 Thr Thr Leu Ala Val Lys Val Thr Cys Phe His Arg Glu Val Ile Val 85 90 95 Phe His Asn Ala Asn Leu Phe Arg Pro Val Phe Glu Gly Thr Gly Leu 100 105 110 Asn Glu Leu Cys Glu Glu Ala Arg Ala Leu Phe Gly Tyr Thr Gln Phe 115 120 125 Ile Glu Pro Gly Pro Pro His Gly Ile Trp Asn Pro Leu Glu Cys Pro 130 135 140 Gln Leu Pro Asp Lys Asp Glu Met Phe Leu Gly Val Val Val Thr Glu 145 150 155 160 Gly Phe Lys Glu Arg Leu Trp Arg Gly Cys Leu Val Pro Ala Val Phe 165 170 175 Gln Thr Gln Gln Val Gln Ile Ala Gly Arg Gln Ala Phe Lys Val Pro 180 185 190 Leu Tyr Asp Glu Asp Leu Phe Ala Pro His Gly His Arg Met Pro Arg 195 200 205 Phe Tyr His Lys Asp Val Ser Ala Tyr Leu Tyr Asn Ser Leu Phe Thr 210 215 220 Ser Ile Ala Gln Ala Leu Arg Leu Lys Asp Val Thr Ala Val Ile His 225 230 235 240 Ala Thr Glu Lys Gln Phe Met Gln Asp His Tyr Lys Ile Ala Lys Ile 245 250 255 Val Gln Ala Lys Gln Phe Ser Thr Thr Leu Pro Lys Thr Ala Asp Gly 260 265 270 Ser Ser His Met Ile Val Asp Ser Val Val Ala Glu Leu Ala Leu Ser 275 280 285 Tyr Gly Cys Met Phe Leu Glu Cys Pro Gln Asp Ala Cys Glu Leu Leu 290 295 300 Asn Tyr Asp Ser Trp Pro Ile Phe Asp Gly Cys Asp Ser Ser Glu Asp 305 310 315 320 Arg Val Asn Ala Leu Glu Arg Trp Ser Ala Glu Gln Ala Val His Val 325 330 335 Ala Gly Gln Leu Phe Ala Ala Asn Ser Val Leu Tyr Leu Thr Arg Val 340 345 350 Gln Lys Gln Ala Pro Arg Gly Gln Lys Gly Asp Val Asn Val Tyr Asn 355 360 365 Ser Phe Phe Leu Gln His Gly Leu Gly Phe Leu Asn Glu Ala Thr Ile 370 375 380 Lys Glu Asn Gly Ser Glu Ala Phe Lys Gly Val Pro Ser Asn Ala Leu 385 390 395 400 Asp Gly Ser Ser Phe Thr Pro Tyr His Leu Ala Tyr Ala Ala Ser Phe 405 410 415 Ser Pro His Leu Leu Ala Lys Leu Cys Tyr Tyr Met Gln Phe Leu Gln 420 425 430 His His Lys Ser Ser Thr Asn Gln Thr Phe Asn Ile Val His Tyr Val 435 440 445 Gly Thr Ala Ala Asn Ser Glu Met Cys Thr Leu Cys His Gly Asp Thr 450 455 460 Pro Gly Thr Cys Leu Asn Thr Leu Phe Tyr Arg Leu Lys Asp Arg Phe 465 470 475 480 Pro Ala Val Thr Thr Pro Gln Arg Arg Asp Pro Tyr Val Val Thr Gly 485 490 495 Thr Ala Gly Thr Phe Asn Asp Leu Glu Ile Leu Gly Asn Phe Ala Ser 500 505 510 Phe Arg Asp Arg Glu Glu Asp Gly Asn Pro Ala Asp Glu His Pro Lys 515 520 525 Tyr Thr Tyr Trp Gln Leu Cys Gln Thr Val Thr Glu Lys Leu Ser Ala 530 535 540 Ile Gly Ile Thr Glu Asp Gln Asp Asn His Val Asn Leu Ile Thr Asn 545 550 555 560 Ile Gln Ser Phe Leu Arg Val Phe Lys Gly Ile Asp Ser Val Val Asp 565 570 575 Gly Glu Val Met Lys Phe Ile Asn Ser Met Ile Lys Asn Asn Phe Asn 580 585 590 Phe Arg Glu His Val Lys Ser Val His His Ile Leu Gln Phe Cys Cys 595 600 605 Asn Val Tyr Trp Gln Ala Pro Cys Ala Val Phe Leu Asn Leu Tyr Tyr 610 615 620 Lys Ser Leu Leu Trp Ile Ile Gln Asp Ile Cys Leu Pro Tyr Cys Met 625 630 635 640 Ile Tyr Glu Gln Asp Asn Pro Ala Met Gly Ile Leu Pro Ser Glu Trp 645 650 655 Leu Lys Met His Phe Gln Thr Leu Trp Thr Asn Phe Lys Ala Ala Cys 660 665 670 Leu Asp Arg Gly Val Leu Thr Gly Cys Glu Leu Lys Ile Val His Arg 675 680 685 Asp Met Phe Cys Asp Phe Phe Asp Thr Asp Ala Gly Ser Asn Gly Leu 690 695 700 Leu Ala Pro Phe Lys Met Gln Val Arg Ile Ala Arg Ala Met Met Val 705 710 715 720 Val Pro Lys Ser Ile Lys Ile Lys Asn Arg Ile Ile Phe Ser Asn Thr 725 730 735 Ala Gly Ser Glu Ala Val Gln Ser Gly Phe Val Lys Pro Thr Gly Thr 740 745 750 Arg Asp Thr Tyr Val Val Ala Gly Pro Tyr Met Lys Phe Leu Asn Ser 755 760 765 Leu His Arg Ala Leu Phe Pro Asn Thr Lys Thr Ala Ala Leu Tyr Leu 770 775 780 Trp His Lys Ile Ser Gln Thr Asn Lys Thr Pro Val Leu Lys Asp Val 785 790 795 800 Pro Asp Asp Glu Leu Ala Glu Leu Val Ser Tyr Val Lys Thr Asn Ser 805 810 815 Leu Ala Phe Glu Glu Thr Asn Val Leu Asp Val Val Pro Asp Ser Leu 820 825 830 Met Ser Tyr Ala Arg Ile Lys Leu Asn Gly Ala Ile Leu Arg Ala Cys 835 840 845 Gly Gln Ile Gln Phe Tyr Ala Thr Thr Leu His Cys Leu Thr Pro Val 850 855 860 Leu Gln Thr Ile Asp Ala Glu Glu Tyr Pro His Val Leu Gly Ser Ala 865 870 875 880 Ala Ile Ala Thr Pro Val Ala Tyr Leu Ser Glu Ile Arg Gly Arg Thr 885 890 895 Ala Leu Thr Val Gln Thr Thr Ala Arg Gln Pro Val Ala Ala Thr Gly 900 905 910 Arg Leu Arg Pro Val Ile Thr Val Pro Met Val Val Asn Lys Tyr Thr 915 920 925 Gly Val Asn Gly Asn Asn Asn Val Phe His Cys Gly Asn Leu Gly Tyr 930 935 940 Phe Ala Gly Arg Gly Val Asp Arg Asn Leu Trp Pro Glu Ser Ser Pro 945 950 955 960 Phe Lys Lys Thr Gly Val Ser Ala Met Leu Arg Lys Arg His Val Met 965 970 975 Met Thr Pro Ile Val Asp Arg Leu Ile Lys Arg Ala Ala Gly Gln Thr 980 985 990 Ile Ser Thr Phe Glu Ala Glu Ser Val Lys Arg Ser Val Gln Ala Leu 995 1000 1005 Leu Glu Asp Lys Asp Asn Pro Asn Leu Leu Lys Ser Val Ile Leu 1010 1015 1020 Glu Leu Ile Arg His Leu Gly Lys Gly Cys Gln Asp Leu Ser Ser 1025 1030 1035 Glu Asp Val Gln Tyr Tyr Leu Gly Asp Tyr Cys Met Leu Thr Asp 1040 1045 1050 Glu Val Leu Phe Thr Leu Asp Asn Ile Ala Gln Ser Gly Val Pro 1055 1060 1065 Trp Thr Phe Glu Asp Ala Gly Ala Leu Ile Glu Asp Arg Gln Asn 1070 1075 1080 Thr Asp Asp Leu Gln Phe Val Asp Ser Asp Asp Ile Ala Thr Ala 1085 1090 1095 Ser Cys Gln Pro Pro Glu Glu Gln Leu Pro Thr Pro Ser Ala Gly 1100 1105 1110 Ala Leu Leu Ala Gly Lys Lys Arg Lys Ile Asn Val Leu Leu Ser 1115 1120 1125 Asp Leu Asp Leu 1130 7 104 PRT Japanese Macaque Herpesvirus 7 Met Val Leu His Glu Leu Phe Phe Cys Gly Val Asp Asp Arg Arg His 1 5 10 15 Val Phe Glu Ser Gln Gly Leu Gly Asp Thr Gly Lys Lys Gly Val Val 20 25 30 Glu Val Arg Ala Asn Val Phe Met Val Lys Pro Arg His Pro Met Pro 35 40 45 Val Arg Cys Glu Gln Val Phe Val Val Gln Arg His Phe Glu Arg Leu 50 55 60 Thr Pro Gly Asp Leu His Leu Leu Gly Leu Lys His Cys Gly Asn Glu 65 70 75 80 Thr Ala Pro Pro Gln Ser Leu Leu Lys Pro Phe Arg His Asp Asn Ala 85 90 95 Lys Glu His Leu Ile Leu Val Arg 100 8 88 PRT Japanese Macaque Herpesvirus 8 Met Ala Pro Phe Ser Leu Ile Leu Ala Tyr Asp Met Arg Glu Ser Gly 1 5 10 15 Thr Thr Ser Ser Thr Phe Val Ser Ser Asn Ala Arg Leu Leu Val Leu 20 25 30 Thr Tyr Asp Thr Ser Ser Ala Ser Ser Ser Ser Gly Thr Ser Phe Arg 35 40 45 Thr Gly Val Leu Leu Val Trp Glu Ile Leu Cys His Arg Tyr Ser Ala 50 55 60 Ala Val Leu Val Phe Gly Asn Ser Ala Arg Trp Ser Glu Phe Arg Asn 65 70 75 80 Phe Met Tyr Gly Pro Ala Thr Thr 85 9 86 PRT Japanese Macaque Herpesvirus 9 Met Gln Arg Cys Gly Val Glu Leu Asn Leu Thr Ala Arg Pro Gln Asn 1 5 10 15 Gly Pro Val Gln Phe Asn Pro Arg Val Arg His Glu Gly Ile Arg Asp 20 25 30 His Val Gln His Val Arg Phe Leu Glu Arg Glu Ala Val Gly Phe Asp 35 40 45 Val Arg His Gln Leu Arg Gln Leu Val Val Arg Asp Val Phe Gln Asp 50 55 60 Trp Gly Phe Val Gly Leu Gly Asp Phe Val Pro Gln Val Gln Arg Gly 65 70 75 80 Gly Leu Gly Val Trp Glu 85 10 83 PRT Japanese Macaque Herpesvirus 10 Met Phe Leu Ala Arg Cys Ser Thr Ser Ser Asp Arg Leu Asp Val Ser 1 5 10 15 Thr Glu Phe Cys Leu Arg Ser Ser Gly Arg Arg Ser Arg Phe Arg Phe 20 25 30 Ser Ile Cys Val Phe Val Phe Arg Met Arg Glu Pro Ser Ile Leu Arg 35 40 45 Gly Ser Ala Lys Thr Thr Arg Leu Arg Ser Thr Ala Arg Ala Asp Ser 50 55 60 Cys Ala Tyr Lys Ala Ala Ser Ser Leu Ala Ile Val Val Arg Arg Pro 65 70 75 80 Arg Phe Ser 11 686 PRT Japanese Macaque Herpesvirus 11 Met Ala Arg Glu Leu Ala Ala Leu Tyr Ala Gln Leu Ser Ala Leu Ala 1 5 10 15 Val Asp Leu Ser Leu Val Val Phe Ala Asp Pro Arg Ser Ile Asp Gly 20 25 30 Ser Arg Ile Leu Lys Thr Lys Thr Gln Ile Glu Asn Leu Asn Arg Asp 35 40 45 Leu Leu Pro Leu Leu Arg Lys Gln Asn Ser Val Glu Thr Ser Ser Leu 50 55 60 Ser Leu Glu Val Glu His Leu Ala Lys Asn Ile Glu Asp Lys Leu Gly 65 70 75 80 Glu Leu Glu Arg Ser Leu Arg Gln Arg Tyr Ser Ser Arg Glu His Phe 85 90 95 Glu Thr Leu His Leu Arg Pro Glu Cys His Tyr His Ala Thr Val Thr 100 105 110 Phe Glu Phe Tyr Gly Gly Gly Leu Ile Asp Val Asn Met Cys Leu Ile 115 120 125 Asn Asp Val Glu Leu Leu Cys Lys Arg Leu Gly Ser Val Phe Tyr Cys 130 135 140 Ile Gly Ala Asn Glu Ala Leu Ser Gly Leu Asp Arg Val Leu Ala Phe 145 150 155 160 Leu Ser Thr Leu Arg Gly Ile Ser Pro Ile Pro His Pro Asp Leu Tyr 165 170 175 Val Thr Ser Val Pro Cys Val Gln Cys Leu Arg Glu Ile Glu Leu Val 180 185 190 Pro Asn Gln Gly Ser Ser Leu Leu Ala Val Leu Ala Asp Arg His Cys 195 200 205 Asp His Leu Cys Lys Lys Val Arg Ala Glu Pro Ile His Gly Leu Phe 210 215 220 Glu Thr Glu Leu Ser Gln Leu Gly Leu Lys Val Ala Lys Gly Ser Asp 225 230 235 240 Ala Thr Gln His Gly Val Arg Ser Ser Ala Asp Gln Leu Arg Glu Ser 245 250 255 Ser Leu Ala Ala Ile Gln Asp His Asn Ile Phe Lys Arg Val Ser Ala 260 265 270 Ser Ile Met Glu Leu Ser Asn Leu Ile Tyr Trp Asn Ala Gly Gln Thr 275 280 285 Gly Leu Gln Thr Gly Thr Glu Asn Glu Cys Ser Gln Met Ala Lys Leu 290 295 300 Leu Thr His Glu Ala Glu Met His Glu His Arg Ala Leu Ile Thr Pro 305 310 315 320 Lys Gln Ser Ala Ala His Phe Tyr Asp Cys Phe Arg Pro Asp Pro Ile 325 330 335 Glu Ser Leu Phe Cys Gly Gly Leu Phe Asn Ser Ile Asp Asp Thr Ile 340 345 350 Asn Ala Leu Ser Arg Asp Cys Ser Val Thr Phe Phe Gln Gln Ala Asn 355 360 365 Tyr Thr Asn Val Met Arg Lys Gln Asn Glu Leu Phe Thr Arg Leu Asn 370 375 380 Ser Ile Leu Cys Gln Gly Ser Ala Gly Ser Gln Lys Pro Ala Thr Pro 385 390 395 400 Ser Glu Pro Arg Thr Ala Thr Val Ala Ala Thr Ala Ala Ser Asp Val 405 410 415 Ile Lys Asp Ala Gln Tyr Arg Lys Glu Gln Tyr Met Lys Lys Val Ala 420 425 430 Arg Asp Gly Phe Lys Lys Leu Thr Glu Cys Leu Gln Thr Gln Ser Ala 435 440 445 Val Leu Ala Asn Ala Leu Cys Met Arg Val Trp Gly Gly Val Ala Tyr 450 455 460 Gly Glu Ala Ser Glu Leu Val Asn His Phe Leu Leu Arg Arg Arg Phe 465 470 475 480 Val Ala Leu Pro Trp Glu Ala Arg Cys Arg Ser Asn Gln Ile Leu Phe 485 490 495 Glu Asn Ser Lys Tyr Ile Lys Asn Ser Leu Tyr Ser Gln Arg Leu Ser 500 505 510 Arg Glu His Val Glu Ile Ile Thr Leu Gln Phe Tyr Gly Leu Ile Thr 515 520 525 Gly Pro Leu Thr Arg Gln Ser Asp Leu Phe Pro Gly Pro Ala Asn Val 530 535 540 Val Leu Ala Gln Cys Phe Glu Ala Ala Gly Met Leu Pro His His Lys 545 550 555 560 Met Leu Val Ser Glu Met Ile Trp Pro Gln Ile Gln Pro Lys Asp Trp 565 570 575 Ile Asp Gln Thr Phe Asn Arg Phe Tyr Gln Leu Pro Glu Gly Asp Leu 580 585 590 Asn Ala Val Gln Lys Ser Ala Trp Cys Phe Ile Arg Glu Leu Val Leu 595 600 605 Ser Val Ala Leu Tyr Asn Arg Thr Trp Glu Lys Thr Leu Arg Ile Phe 610 615 620 Ser Leu Ala Arg Glu Lys Pro Ser Ile Ser Asp Leu Asp Val Lys Ser 625 630 635 640 Leu Thr Pro Gly Leu Tyr Leu Thr Tyr Glu Gln Asn Thr Pro Leu Val 645 650 655 Leu Ile Ser Gln Asn Thr Gly Trp Ile Phe Lys Asp Leu Tyr Ala Leu 660 665 670 Leu Tyr His His Leu Gln Leu Ser Asp Gly His Asp Asp Asn 675 680 685 12 107 PRT Japanese Macaque Herpesvirus 12 Met Trp Gly Thr Ile Phe Phe Leu Asn Thr Ile Arg Met Pro Ser Trp 1 5 10 15 Cys Val Leu Ser Ser Val Pro Gly His Val Phe Ser Arg Leu Asn Leu 20 25 30 Lys Ser Ser Pro Val Ala Glu Ala Leu His Thr Arg Asn Leu Asn Ala 35 40 45 Ser Ala Leu Gly Gly Phe Ser Gly Gly Val Gly Val Asp Gly Pro Gly 50 55 60 Val Asp Phe Ala Val Val Val Thr Pro Phe Gly Val Val Thr Phe Ser 65 70 75 80 Pro Thr Ala Ala Pro Ile Ala Ile Ile Thr Thr His Ala Arg Ser Arg 85 90 95 Arg Arg Val Arg Leu Val Ile Ile Met Ala Val 100 105 13 828 PRT Japanese Macaque Herpesvirus 13 Met Met Ile Thr Asn Arg Thr Arg Arg Leu Leu Arg Ala Trp Val Val 1 5 10 15 Ile Ile Ala Ile Gly Ala Ala Val Gly Glu Asn Val Thr Thr Pro Lys 20 25 30 Gly Val Thr Thr Thr Ala Lys Ser Thr Pro Gly Pro Ser Thr Pro Thr 35 40 45 Pro Pro Glu Asn Pro Pro Arg Ala Glu Ala Phe Lys Phe Arg Val Cys 50 55 60 Ser Ala Ser Ala Thr Gly Glu Leu Phe Arg Phe Asn Leu Glu Lys Thr 65 70 75 80 Cys Pro Gly Thr Glu Asp Lys Thr His Gln Glu Gly Ile Leu Met Val 85 90 95 Phe Lys Lys Asn Ile Val Pro His Ile Phe Lys Val Arg Arg Tyr Arg 100 105 110 Lys Val Ala Thr Ser Val Thr Val Tyr Arg Gly Trp Thr Glu Thr Ala 115 120 125 Val Thr Gly Lys Gln Glu Val Ile Arg Pro Val Pro Gln Tyr Glu Ile 130 135 140 Asn His Met Asp Thr Thr Tyr Gln Cys Phe Ser Ser Met Arg Val Asn 145 150 155 160 Val Asn Gly Ile Glu Asn Thr Tyr Thr Asp Arg Asp Phe Thr Asn Gln 165 170 175 Thr Val Phe Leu Gln Pro Val Glu Gly Leu Thr Asp Asn Ile Gln Arg 180 185 190 Tyr Phe Ser Gln Pro Val Leu Tyr Thr Thr Pro Gly Trp Phe Pro Gly 195 200 205 Ile Tyr Arg Val Arg Thr Thr Val Asn Cys Glu Ile Val Asp Met Ile 210 215 220 Ala Arg Ser Ala Glu Pro Tyr Ser Tyr Phe Val Thr Ala Leu Gly Asp 225 230 235 240 Thr Val Glu Val Ser Pro Phe Cys Leu Asn Asp Ser Thr Cys Ser Val 245 250 255 Ala Asp Lys Ala Glu Asn Gly Leu Gly Val Arg Val Leu Thr Asn Tyr 260 265 270 Thr Ile Val Asp Phe Ala Thr Arg Thr Pro Thr Thr Glu Thr Arg Val 275 280 285 Phe Ala Asp Ser Gly Glu Tyr Thr Val Ser Trp Lys Ala Glu Asp Pro 290 295 300 Lys Ser Ala Val Cys Ala Leu Thr Leu Trp Lys Thr Phe Pro Arg Ala 305 310 315 320 Ile Gln Thr Thr His Glu Ala Ser Tyr His Phe Val Ala Asn Asp Val 325 330 335 Thr Ala Thr Phe Thr Ser Pro Leu Ser Glu Val Ala Asn Phe Thr Gly 340 345 350 Thr Tyr Ser Cys Leu Asp Asn Val Ile Gln Lys Thr Leu Asn Ala Thr 355 360 365 Ile Lys Lys Leu Ser Asp Thr His Ala Ala Asn Gly Ser Ala Gln Tyr 370 375 380 Tyr Glu Thr Glu Gly Gly Leu Phe Leu Leu Trp Gln Pro Leu Thr Gln 385 390 395 400 Leu Ser Leu Val Asp Glu Met Arg Gly Leu Asn Asp Thr Thr Pro Ala 405 410 415 Pro Pro Thr Thr Ser Thr Ala Ser Arg Val Arg Arg Ser Val Asp Thr 420 425 430 Asn Ser Gln Thr Ala Glu Asp Leu Ala Ala Pro Gln Leu Gln Phe Ala 435 440 445 Tyr Asp Lys Leu Arg Ala Ser Ile Asn Lys Val Leu Glu Glu Leu Ser 450 455 460 Arg Ala Trp Cys Arg Glu Gln Val Arg Asp Thr Tyr Met Trp Tyr Glu 465 470 475 480 Leu Ser Lys Ile Asn Pro Thr Ser Val Met Thr Ala Ile Tyr Gly Arg 485 490 495 Pro Val Ser Ala Lys Phe Val Gly Asp Ala Ile Ser Val Thr Asp Cys 500 505 510 Val Thr Val Asp Gln Gly Ser Val Ser Ile His Lys Ser Leu Arg Thr 515 520 525 Ser Thr Pro Gly Ile Cys Tyr Ser Arg Pro Pro Val Thr Phe Arg Phe 530 535 540 Leu Asn Ser Thr Thr Leu Phe Lys Gly Gln Leu Gly Pro Arg Asn Glu 545 550 555 560 Ile Ile Leu Thr Asp Asn Gln Val Glu Ala Cys Lys Glu Thr Cys Glu 565 570 575 His Tyr Phe Ile Ala Ser Asn Val Thr Tyr Tyr Tyr Lys Asp Tyr Val 580 585 590 Phe Val Lys Lys Ile Asn Thr Ser Glu Ile Ser Thr Leu Gly Thr Phe 595 600 605 Ile Ala Leu Asn Leu Ser Phe Ile Glu Asn Ile Asp Phe Arg Val Ile 610 615 620 Glu Leu Tyr Ser Arg Ala Glu Lys Lys Leu Ser Gly Ser Val Phe Asp 625 630 635 640 Ile Glu Thr Met Phe Arg Glu Tyr Asn Tyr Tyr Thr Gln Arg Leu Ala 645 650 655 Gly Leu Arg Glu Asp Leu Asp Asn Thr Ile Asp Leu Asn Arg Asp Arg 660 665 670 Leu Ala Arg Asp Leu Ser Asp Ile Val Ala Asp Leu Gly Asp Val Gly 675 680 685 Arg Thr Val Val Asn Val Ala Ser Ser Val Ile Thr Leu Phe Gly Ser 690 695 700 Ile Val Ser Gly Phe Ile Asn Phe Ile Lys Ser Pro Phe Gly Gly Met 705 710 715 720 Leu Met Ile Leu Val Ile Val Ala Val Ile Leu Ile Val Phe Ala Leu 725 730 735 Asn Arg Arg Thr Asn Ala Ile Ala Gln Ala Pro Ile Arg Met Ile Tyr 740 745 750 Pro Asp Ile Asp Lys Met Gln Pro Ser Gly Gly Lys Val Asp Gln Glu 755 760 765 Gln Ile Lys Asn Ile Leu Ala Gly Met His Gln Leu Gln Gln Glu Glu 770 775 780 Arg Arg Arg Leu Asp Glu Lys Gln Arg Ser Ala Pro Ser Leu Phe Arg 785 790 795 800 Arg Ala Ser Asp Gly Leu Lys Arg Arg Phe Arg Gly Tyr Lys Pro Leu 805 810 815 Glu Asn Glu Glu Ala Gln Glu Tyr Glu Met Asn Lys 820 825 14 97 PRT Japanese Macaque Herpesvirus 14 Met Gly Ala Trp Ala Met Ala Leu Val Arg Arg Phe Ser Ala Asn Thr 1 5 10 15 Ile Arg Met Thr Ala Thr Ile Thr Arg Ile Met Ser Met Pro Pro Asn 20 25 30 Gly Leu Phe Ile Lys Leu Met Asn Pro Leu Thr Ile Asp Pro Asn Arg 35 40 45 Val Ile Thr Leu Leu Ala Thr Leu Thr Thr Val Arg Pro Thr Ser Pro 50 55 60 Arg Ser Ala Thr Ile Ser Asp Arg Ser Arg Ala Arg Arg Ser Arg Phe 65 70 75 80 Arg Ser Ile Val Leu Ser Arg Ser Ser Arg Ser Pro Ala Ser Arg Cys 85 90 95 Val 15 1012 PRT Japanese Macaque Herpesvirus 15 Met Asp Phe Phe Asn Pro Tyr Leu Gly Pro Arg Gly Pro Arg Pro Pro 1 5 10 15 Ser His Lys Cys Thr Asp Ala Pro Ala Pro Ala Gly Ala Val Gln Pro 20 25 30 Pro Pro Asp Val Cys Arg Leu Ile Pro Ala Cys Leu Arg Thr Pro Gly 35 40 45 Ala Gly Gly Met Ile Pro Val Thr Ile Pro Phe Pro Pro Thr Tyr Phe 50 55 60 Glu Asn Gly Ala Arg Gly Asp Val Leu Leu Ala His Glu Arg Ser Met 65 70 75 80 Trp Thr Ala Arg Gly Gln Arg Pro Val Val Pro Asp Pro Gln Asp Gln 85 90 95 Ser Ile Thr Phe His Ala Tyr Asp Val Val Glu Thr Thr Tyr Ala Ala 100 105 110 Asp Arg Cys Ala Glu Val Pro Ser Arg Phe Gln Thr Asp Ile Ile Pro 115 120 125 Ser Gly Thr Val Leu Lys Leu Leu Gly Arg Thr Glu Asn Gly Thr Ser 130 135 140 Val Cys Val Asn Val Phe Arg Gln Gln Val Tyr Phe Tyr Ala Lys Val 145 150 155 160 Pro Ala Gly Val Asn Val Thr His Val Leu Gln Gln Ala Leu Lys Asn 165 170 175 Thr Ala Gly Arg Ala Ala Cys Gly Phe Ser Thr Arg Arg Val Thr Lys 180 185 190 Lys Ile Leu Lys Thr Tyr Asp Val Ala Glu His Pro Val Thr Glu Ile 195 200 205 Thr Leu Ser Ser Gly Ser Met Leu Ser Thr Leu Ser Asp Arg Leu Val 210 215 220 Ala Cys Gly Cys Glu Val Phe Glu Ser Asn Val Asp Ala Val Arg Arg 225 230 235 240 Phe Val Leu Asp His Gly Phe Thr Thr Phe Gly Trp Tyr Ser Cys Ala 245 250 255 Arg Ala Thr Pro Arg Leu Ala Ala Arg Asp Ala Arg Thr Ala Leu Glu 260 265 270 Phe Asp Cys Ser Trp Glu Asp Leu Ser Val Gln Ala Asp Arg Ser Asp 275 280 285 Trp Pro Pro Tyr Arg Ile Val Ala Phe Asp Ile Glu Cys Met Gly Glu 290 295 300 Ala Gly Phe Pro Cys Ala Thr Arg Asp Gly Asp Ala Val Ile Gln Ile 305 310 315 320 Ser Cys Val Phe Tyr Thr Thr Arg Glu Gly Ala Pro Asn Pro Pro Asn 325 330 335 Ile Leu Phe Ser Val Gly Thr Cys Asp Pro Ile Pro Asp Thr Asp Val 340 345 350 Leu Glu Phe Pro Ser Glu Tyr Asp Met Leu Val Ser Phe Phe Ala Met 355 360 365 Leu Arg Asp Phe Glu Val Asp Phe Leu Thr Gly Tyr Asn Ile Ser Asn 370 375 380 Phe Asp Leu Pro Tyr Leu Ile Thr Arg Ala Ser Gln Val Tyr Asn Leu 385 390 395 400 Arg Leu Asn Glu Tyr Thr Lys Ile Lys Thr Gly Ser Ile Phe Glu Val 405 410 415 His Glu Pro Arg Gly Gly Gly Gly Gly Phe Met Arg Ser Val Ser Lys 420 425 430 Ile Lys Ile Ala Gly Ile Val Pro Ile Asp Met Tyr Gln Val Cys Arg 435 440 445 Glu Lys Leu Ser Leu Ser Asp Tyr Lys Leu Asp Thr Val Ala Arg Gln 450 455 460 Cys Leu Gly Gly Lys Lys Glu Asp Val Ser Tyr Lys Asp Ile Pro Pro 465 470 475 480 Leu Phe Arg Ser Gly Pro Gly Gly Arg Ala Lys Val Gly Ser Tyr Cys 485 490 495 Val Met Asp Ser Val Leu Val Met Asp Leu Leu Lys Met Phe Met Ile 500 505 510 His Val Glu Ile Ser Glu Ile Ala Lys Leu Ala Lys Ile Gln Ala Arg 515 520 525 Arg Val Leu Thr Asp Gly Gln Gln Leu Arg Val Phe Ser Cys Leu Leu 530 535 540 Glu Ala Ala Ala Arg Asp Asn Phe Ile Leu Pro Val Pro Thr Pro Glu 545 550 555 560 Gly Gln Gly Gly Tyr Gln Gly Ala Thr Val Ile Asn Pro Ile Pro Gly 565 570 575 Phe Tyr Asp Glu Pro Val Leu Val Val Asp Phe Ala Ser Leu Tyr Pro 580 585 590 Ser Ile Ile Gln Ala His Asn Leu Cys Tyr Ser Thr Met Ile His Gly 595 600 605 Arg Asp Leu His Leu His Pro Asn Leu Thr Pro Asp Asp Tyr Glu Thr 610 615 620 Phe Val Leu Ser Gly Gly Pro Val His Phe Val Lys Lys His Lys Arg 625 630 635 640 Glu Ser Leu Leu Gly Arg Leu Leu Thr Val Trp Leu Glu Lys Arg Arg 645 650 655 Ala Ile Arg Arg Thr Leu Ala Ala Cys Asp Asp Pro Ser Leu Lys Thr 660 665 670 Ile Leu Asp Lys Gln Gln Leu Ala Ile Lys Val Thr Cys Asn Ala Val 675 680 685 Tyr Gly Phe Thr Gly Val Ala Ser Gly Leu Leu Pro Cys Ile Asn Ile 690 695 700 Ala Glu Thr Val Thr Leu Arg Gly Arg Thr Met Leu Glu Met Ser Lys 705 710 715 720 Ser Tyr Val Glu Ala Leu Thr Thr Asp Asn Leu Arg Thr Arg Leu Gly 725 730 735 Arg Glu Val Thr Ala Cys His Gly Ala Arg Phe Arg Val Val Tyr Gly 740 745 750 Asp Thr Asp Ser Leu Phe Ile Ala Cys Asp Gly Tyr Ser Ala Glu Ala 755 760 765 Val Ser Ala Phe Cys Asp Asp Leu Ala Ala Arg Ile Thr Ala Asp Leu 770 775 780 Phe Pro Pro Pro Ile Lys Leu Glu Ala Glu Lys Thr Phe Lys Cys Leu 785 790 795 800 Leu Leu Leu Thr Lys Lys Arg Tyr Ile Gly Val Leu Leu Asn Asp Lys 805 810 815 Met Val Met Lys Gly Val Asp Leu Ile Arg Lys Thr Ala Cys Lys Phe 820 825 830 Val Gln Glu Arg Cys Arg Ser Ile Leu Asp Leu Val Leu His Asn Gln 835 840 845 Glu Val Lys Ala Ala Ala Arg Leu Leu Cys Lys Arg Pro Pro His Ala 850 855 860 Val Tyr Glu Glu Gly Leu Pro Ala Gly Phe Ile Lys Ile Val Glu Val 865 870 875 880 Leu Asn Ala Ser Tyr Val Asp Leu Arg Asn Ser Val Val Pro Ile Glu 885 890 895 Gln Leu Thr Phe Ser Thr Glu Leu Ser Arg Pro Val Cys Asp Tyr Lys 900 905 910 Thr Thr Asn Leu Pro His Leu Ala Val Tyr Gln Lys Leu Ala Ser Arg 915 920 925 Cys Glu Glu Leu Pro Gln Val His Asp Arg Ile Pro Tyr Val Phe Val 930 935 940 Asp Ala Pro Gly Ala Leu Lys Ser Asp Leu Ala Glu His Pro Asp Tyr 945 950 955 960 Val Lys Gln His Gln Ile Pro Val Ala Val Asp Leu Tyr Phe Asp Lys 965 970 975 Leu Val His Gly Ala Ala Asn Ile Leu Gln Cys Leu Phe Gly Asn Asn 980 985 990 Ala Asp Thr Thr Val Ala Ile Leu Tyr Asn Phe Leu Asn Val Pro Tyr 995 1000 1005 Lys Leu Phe Ser 1010 16 186 PRT Japanese Macaque Herpesvirus 16 Met Leu Arg Asp Val Val Arg Phe Glu Asn Phe Phe Gly Tyr Ser Ser 1 5 10 15 Gly Arg Glu Ala Ala Arg Gly Pro Ala Gly Gly Val Leu Glu Gly Leu 20 25 30 Leu Glu Asp Val Gly Asp Val Asp Ala Gly Trp Asp Leu Arg Val Glu 35 40 45 Ile Tyr Leu Leu Thr Glu His Val His Ala His Ala Gly Ala Val Leu 50 55 60 Gly Ser Pro Gln Glu Leu Glu His Gly Ser Ala Arg Asn Asn Val Arg 65 70 75 80 Leu Glu Ala Ala Arg Tyr Leu Gly Ala Pro Val Arg Arg Val Arg Arg 85 90 95 Phe Asn Asp Val Val Arg Val Lys Arg Asn Gly Leu Val Leu Gly Val 100 105 110 Arg Asp Asp Trp Pro Leu Ala Ala Arg Arg Pro His Gly Pro Phe Val 115 120 125 Gly Glu Gln His Val Ser Ala Arg Ala Val Phe Lys Val Arg Arg Arg 130 135 140 Glu Arg Asp Arg Asp Arg Asp His Pro Ala Cys Pro Arg Arg Ser Glu 145 150 155 160 Ala Gly Gly Asn Glu Pro Ala Asp Val Trp Trp Arg Leu Asn Gly Ala 165 170 175 Gly Gly Gly Gly Arg Ile Gly Ala Phe Val 180 185 17 102 PRT Japanese Macaque Herpesvirus 17 Met His Arg Ser Ala Ala Gln His Glu Arg Leu Val Val Val Arg Arg 1 5 10 15 Gln Val Gly Val Gln Val Gln Val Ser Ser Val Tyr His Gly Gly Val 20 25 30 Ala Gln Val Val Arg Leu Asp Asp Ala Trp Val Gln Ala Gly Lys Ile 35 40 45 Asp His Gln Asp Arg Leu Val Val Lys Pro Arg Asp Gly Val Asn His 50 55 60 Arg Arg Ala Leu Ile Thr Pro Leu Ser Leu Gly Arg Trp Asp Arg Glu 65 70 75 80 Asp Lys Val Ile Pro Gly Arg Gly Leu Gln Gln Ala Gly Glu His Ala 85 90 95 Lys Leu Leu Ala Val Arg 100 18 101 PRT Japanese Macaque Herpesvirus 18 Met Pro Leu His Pro Gly Pro Gly Ala Pro Gln Ser Gly Gly Gln Gly 1 5 10 15 Gly Gly Ala Ala Val Val Gln Ala Thr Ala Ala Arg Gly Ile Arg Gly 20 25 30 Gly Val Ala Gly Gly Leu Tyr Lys Asn Cys Gly Gly Pro Gln Arg Glu 35 40 45 Leu Cys Gly Pro Ser Lys Gln Arg Arg Ala His Arg Ala Val Asn Val 50 55 60 Leu Asp Arg Ala Gln Pro Pro Arg Leu Arg Leu Gln Asp His Gln Pro 65 70 75 80 Ala Pro Pro Gly Gly Val Pro Glu Ala Gly Glu Gln Val Arg Gly Ala 85 90 95 Ala Pro Gly Ala Arg 100 19 416 PRT Japanese Macaque Herpesvirus 19 Met Leu Val Asn Glu Leu Ser Met Val Leu Gly Asp Trp Glu Val Thr 1 5 10 15 Phe His Arg Gly Lys Phe Ser Phe Val Asn Leu Ala Arg Leu Gln Thr 20 25 30 Phe Lys Gly His Gly Gly Tyr Ala Lys Ile Arg Leu Pro Phe Ser Leu 35 40 45 Asp Gln Leu Leu His Gln His Phe Ala Phe Gly Leu Val Thr Arg Leu 50 55 60 Asn Glu Leu Pro Pro Phe Ser Asp Cys Val Ala Leu Ile Ala Pro Arg 65 70 75 80 Asp Ser Gly Gly Asp Ala Asp Ala Ala Arg Val Ala Pro Gly Phe Val 85 90 95 Leu Asp Ser Ser Arg Pro Leu Thr Val Trp Val Asn Ala Asn Gly Arg 100 105 110 His Thr Val Arg Phe Cys Leu Leu Phe Leu Lys Pro Ile Asp Leu Glu 115 120 125 Arg Ala Val Thr Tyr Val Phe Gly Glu Asn Gly Gly Ala Arg Ser Glu 130 135 140 Gly Ala Pro Lys Pro Thr Cys Asn Thr Glu Ser Leu Pro Gly Gly Pro 145 150 155 160 Leu Arg Val Ser Gly Glu Ala Ser Gln Thr Ser Pro His Ser Phe Val 165 170 175 Ala Tyr Phe Pro Thr Ala Asp Pro Val Ala Cys Leu Ser Leu Leu Arg 180 185 190 Leu Gln Val Arg Pro Phe Ser Asp Asp Ala Ala His Arg Asp Ala Arg 195 200 205 Ile Ser Pro Lys Tyr Val Thr Phe Ser Asn Ala Gly Gly Asn Val Cys 210 215 220 Lys Ala Ser Val His Thr Leu Ser Pro Ser Arg Cys Lys Thr Ala Gln 225 230 235 240 Met Glu Ile Ile Tyr Ala Pro Gly Asp Pro Asn Ala Glu Ile Val Leu 245 250 255 Gly Gln Ser Gly Pro Val Leu Pro Thr His Thr Gly Gly Arg Val Leu 260 265 270 Gly Val Tyr Ala Asp Ala Glu Lys Thr Ile Gln Pro Gly Ser Ser Ala 275 280 285 Glu Val Arg Val Gln Leu Ile Phe Gln Gln Gly Ala Ala Ala Arg Gly 290 295 300 Asp Leu Ala Phe Leu Val Ala Gly Val Ala Pro Glu Pro Leu Phe Ile 305 310 315 320 Val Thr Pro Thr Leu Leu Leu Ser Gly Cys Thr Thr His Leu Arg Leu 325 330 335 Phe Asn Pro Asn Gly Thr Pro Thr Thr Ile Lys Arg Asp Thr Leu Val 340 345 350 Ala Ala Ala Ala Pro Cys Pro Val Val Arg Val Ser Ser Ala Asp Asp 355 360 365 Ala Pro Arg Asp Leu Val Ala Ser Pro Asp Thr Gly Ala Leu Ser Ile 370 375 380 Asp Ala Phe Thr Ile Pro Val Gly Leu Pro Gly Val Val Ser Ala Glu 385 390 395 400 Cys His Val Ser Met Arg Asp Asn Gly Val His Glu Arg Met Ser His 405 410 415 20 91 PRT Japanese Macaque Herpesvirus 20 Met Glu Ser Ala Pro Val Ser Gly Asp Ala Thr Arg Ser Arg Gly Ala 1 5 10 15 Ser Ser Ala Glu Leu Thr Arg Thr Thr Gly Gln Gly Ala Ala Ala Ala 20 25 30 Thr Arg Val Ser Leu Phe Ile Val Val Gly Val Pro Leu Gly Leu Asn 35 40 45 Arg Arg Arg Cys Val Val Gln Pro Glu Ser Lys Ser Val Gly Val Thr 50 55 60 Met Asn Arg Gly Ser Gly Ala Thr Pro Ala Thr Arg Asn Ala Arg Ser 65 70 75 80 Pro Arg Ala Ala Ala Pro Cys Trp Lys Ile Asn 85 90 21 409 PRT Japanese Macaque Herpesvirus 21 Met Gly Thr Pro Val Arg Phe Phe Arg Gly Glu Trp Gln Thr Ser Ser 1 5 10 15 Leu Val Asp Asn Gly Thr Pro Arg Tyr Ser Ser Leu Val Trp Ala Ala 20 25 30 Thr Ile His Asp Gly Tyr Leu Thr Leu Val Asn Arg Ser Glu Leu Cys 35 40 45 Val Thr Glu Arg Ser Pro Cys Leu Pro Ala Cys Pro Ser Ile Gly Arg 50 55 60 Leu Val Gly Lys Arg Phe Pro Gly Phe Ala Phe Ala Ser Ala Thr Leu 65 70 75 80 Gly Asp Arg Gly Thr Arg Thr Val Phe Tyr Ala Phe Gly His Arg Asp 85 90 95 Asn Pro Leu Asp Ile Val Pro Ala Val Val Glu Arg Ala Asp Arg Glu 100 105 110 Leu Val Leu Arg Val His Ala Pro Arg Thr Thr Arg Val Ser Arg Tyr 115 120 125 Gly Leu Lys Ile Phe Val Ala Ile Val Thr Val Val Arg Pro Pro Gly 130 135 140 Val Phe Leu His Phe Pro Gln Asp Arg Val Pro Ile Ala Leu Thr Asp 145 150 155 160 Ala Cys Ser Gln Glu Gly Ser Arg Leu Thr Ser Glu Glu Pro Trp Ile 165 170 175 Lys Ile Gln Gly Phe Pro Val Leu Ser Asp Glu Thr Ala His Pro Phe 180 185 190 Leu Leu Thr Gln Lys Thr Lys Pro Phe Thr Glu Arg Lys Phe Cys Arg 195 200 205 Leu Ile Met Asp Asp Asn Gln Leu Ser Ala Val Asn Thr Val Tyr Leu 210 215 220 Gly Lys Gln His Val Arg Val Thr Val Thr Arg Pro Pro Glu Thr Ile 225 230 235 240 Val Thr Asp Gly Pro Val Thr Ala Thr Leu Ser Leu Thr Gly Asn Ala 245 250 255 Pro Ile Ala Phe Arg His Asn Pro Tyr Phe Glu Leu Pro Trp Ser Ser 260 265 270 Thr Thr Ala Ile Phe Thr Pro Val Val Tyr Val Gly Leu Thr Val Cys 275 280 285 Ile Pro Pro Asn Cys Ser Lys Phe Val Arg Tyr Gly Asn Thr Tyr Val 290 295 300 Ser Ala Phe Asn Arg Lys Leu Thr Ala Ile Ile Ser Asn His Ala His 305 310 315 320 Asp Gly Gly Phe Arg Ile Gln Asp Cys Glu Trp Pro Pro Asn Arg Glu 325 330 335 Ile Glu Ile Leu Val Thr Asn Val Thr Gln Ala Pro Val Tyr Val Ser 340 345 350 Thr Gly Thr Gln Leu Gly Arg Ala Ile Phe Val Phe Ala Pro Arg Phe 355 360 365 Gly Gly Pro Ala Lys Leu Arg Gln Leu Leu Gly His Arg Ser Arg Ala 370 375 380 Leu Glu Leu Pro Gly Gly Val Thr Val Asp Ser Gln Lys Leu Cys Arg 385 390 395 400 Phe Glu Thr Met Tyr Leu Phe Ser Thr 405 22 207 PRT Japanese Macaque Herpesvirus 22 Met Phe Pro Val Trp Phe Val Leu Phe Tyr Leu Ser Cys Trp Ala Ala 1 5 10 15 Ser Pro Thr Leu Ala Pro Pro Pro Thr Ala Ala Gly Ile Asn Val Leu 20 25 30 Pro Gln Trp Ala Gly Asn Arg Ala Ser Leu Asp Arg Thr Arg Gly Arg 35 40 45 Leu Ser Glu Leu Gly Leu Asn Ile Gln Arg Trp Phe Val Tyr Leu Cys 50 55 60 Tyr His Ser Thr Leu Cys Arg Val Arg Glu Tyr Pro Arg Ile Met Ser 65 70 75 80 Phe Ile Asn Phe Pro Ile Leu Met Ser Asn Val Glu Cys Gln Arg Arg 85 90 95 Glu Phe Arg Gly Ala Glu Cys Met Asn Ala Met Val Arg Gly Leu Arg 100 105 110 Ala Tyr Glu Ser Tyr Leu Thr Arg Ser Lys Met Leu Leu Asp Asp Ala 115 120 125 Pro Gly Asn Ala Gly Ala Ala Ala Ile Gly Ser Ala Val Thr Val Val 130 135 140 Leu Ser Ala Leu Asn Ser Leu Ile Glu Glu Leu Pro Val Asp Asn Lys 145 150 155 160 Ile Gly Gly Val Glu Ser Asn Asp Lys Ile Val Arg Ala Leu Ala Glu 165 170 175 Gln Ser Pro Gly Asp Val Ile Leu Ser Ala Phe Arg Leu Leu Glu Tyr 180 185 190 Leu Gln Met Phe Leu Arg Asp Gly Arg Arg Ala Ile Ala Met Met 195 200 205 23 333 PRT Japanese Macaque Herpesvirus 23 Met Ile Val Leu Val His Leu Gly Ile Cys Tyr Val Lys Lys Ile Ile 1 5 10 15 Pro Ala Cys Leu Ser Gly Ile Ala Ala Val Arg Cys Arg Val Ser Arg 20 25 30 Gly Ser Glu Val Ala Ala Ala Arg Ala Pro Asp Gly Arg Gly Glu His 35 40 45 Gly Glu Leu Gln Tyr Leu Ala His Leu Asp Leu Ile Ile Arg His Gly 50 55 60 Val Gln Arg Asp Asp Arg Thr Gly Val Gly Thr Arg Ser Val Phe Gly 65 70 75 80 Leu Gln Ala Arg Tyr Asn Leu Arg Asp Glu Phe Pro Leu Leu Thr Thr 85 90 95 Lys Arg Val Phe Trp Arg Gly Val Val Glu Glu Leu Leu Trp Phe Ile 100 105 110 Arg Gly Ser Thr Asp Ser Thr Glu Leu Ser Arg Arg Gly Val Lys Ile 115 120 125 Trp Asp Ala His Gly Ser Arg Ala Phe Leu Ala Ala Gln Gly Phe Gly 130 135 140 Asp Arg Arg Glu Gly Asp Leu Gly Pro Val Tyr Gly Phe Gln Trp Arg 145 150 155 160 His Phe Gly Ala Glu Tyr Arg Gly Ala Asp Ala Asp Tyr Glu Gly Gln 165 170 175 Gly Val Asp Gln Leu Arg Tyr Val Val Asp Leu Ile Val Arg Arg Pro 180 185 190 His Asp Arg Arg Ile Val Met Cys Ala Trp Asn Pro Ala Asp Leu Ala 195 200 205 Arg Met Ala Leu Pro Pro Cys His Val Leu Cys Gln Phe Tyr Val Ala 210 215 220 Arg Gly Glu Leu Ser Cys Gln Leu Tyr Gln Arg Ser Ala Asp Met Gly 225 230 235 240 Leu Gly Val Pro Phe Asn Ile Ala Ser Tyr Ala Leu Leu Thr Tyr Leu 245 250 255 Ile Ala His Val Thr Gly Leu Thr Pro Gly Asp Phe Val His Thr Leu 260 265 270 Gly Asp Ala His Val Tyr Asn Asn His Val Gly Pro Leu Leu Leu Gln 275 280 285 Leu Gly Arg Thr Pro Arg Pro Phe Pro Arg Leu Lys Ile Leu Arg Lys 290 295 300 Val Thr Arg Leu Glu Asp Phe Thr Arg Ala Asp Leu Ser Leu Glu Gly 305 310 315 320 Tyr Asp Pro His Pro His Ile Glu Met Glu Met Ala Val 325 330 24 88 PRT Japanese Macaque Herpesvirus 24 Met Cys Leu His Gly Gly Ala Ser Thr Met Thr Leu Lys Ile Asn Val 1 5 10 15 Phe Cys Gly Ser Cys Thr Met Arg Val Trp Leu Met Asn Ala Gly Gly 20 25 30 Asp Ser Gly Gly Asp Ala Gly Gly Asp Ser Gly Gly Asp Ala Gly Gly 35 40 45 Asp Ser Gly Gly Asp Ala Gly Gly Asp Ser Gly Gly Asp Ala Gly Gly 50 55 60 Asp Ser Gly Gly Asp Ala Gly Gly Asp Ser Gly Gly Asp Ala Gly Glu 65 70 75 80 Gly Pro Arg Gly Phe Thr Thr Arg 85 25 120 PRT Japanese Macaque Herpesvirus 25 Met Arg Val Leu Val Ile Gly Ala Phe Phe Ala Val Phe Ala Cys Val 1 5 10 15 Val Asp Tyr Ala Phe Pro Met Gly Ser Met Ser Gly Pro Ala Pro Glu 20 25 30 Val Cys Cys Leu Gly Tyr Ile Asn Lys Leu Pro Pro Ser Gly Ala Val 35 40 45 Ala Leu Tyr Tyr Tyr Thr Ser Ser Gln Cys Thr Leu Asp Ala Val Ile 50 55 60 Leu Glu Thr His Arg Gly Gln Lys Leu Cys Ala Asn Pro Gly Asp Asp 65 70 75 80 Gly Val Arg Lys Leu Leu Gln Lys Val Asp Asn Arg Pro Lys Arg Asn 85 90 95 Lys Gly Arg Arg Thr Arg Arg Ser Leu Leu Asp Asp Ala Ser Asp Glu 100 105 110 Gly Leu Glu Ser Gly Ser Gly Phe 115 120 26 91 PRT Japanese Macaque Herpesvirus 26 Met Arg Arg Val Cys Leu Gly Gly Gly Asp Phe Pro Phe Ile Ala Gly 1 5 10 15 Thr Gly Pro Leu Leu Val Leu Glu Ile Pro Phe Ser Thr Gly Ser Leu 20 25 30 Leu Arg Arg Lys Ala Val Tyr Leu Phe Gly Glu Ser Pro Phe Phe Arg 35 40 45 Thr Pro Gly Ala Thr Val Val Arg His Ala Arg Phe Gly Thr Arg Asp 50 55 60 Ala Thr Ser Gly Arg Glu Ala Arg Ala Pro Gly Gly Trp Pro Arg Leu 65 70 75 80 Val Ser Val Glu Ala Asp Pro Gly Arg Gly Tyr 85 90 27 112 PRT Japanese Macaque Herpesvirus 27 Met Leu Phe Leu Val Ala Ile Gly Asp Ile Phe Arg Cys Pro Pro Asn 1 5 10 15 Asp Pro Val Arg Arg Gly Phe Phe Gly Ser Phe Gly Gly His Arg Lys 20 25 30 Met Phe Pro Arg Ala Arg Arg Ala Thr Val Glu Thr Ile Phe Ser Asp 35 40 45 Pro Leu Val Thr Pro Glu Pro Ala Pro Pro Arg Gly Ala Pro Cys Leu 50 55 60 Gly Ala Glu Gln Ser Val Leu Val Arg Thr Pro Asn Ala Gly Leu Ala 65 70 75 80 Val Pro Thr Pro Ala Arg Lys Thr Arg Gly Thr Pro Ala Gly Phe Tyr 85 90 95 Ala Ile Thr Leu Cys Tyr Phe Gly Val Gly Ala Pro Arg Cys Pro Cys 100 105 110 28 102 PRT Japanese Macaque Herpesvirus 28 Met Ser Gly Val Ser Val Thr Arg Gly Ala Glu Ala Ala Gly Gly Gly 1 5 10 15 Val Gly Lys Asn Ser Gly Arg Arg Ala Arg Val Ser Val Met Thr Arg 20 25 30 Leu Asp Gly Gly His Leu Ala Ala Gly Gln Arg Arg Glu His Arg Glu 35 40 45 Arg Pro Ala Gly Gly Ala Ala Arg Asp Arg Ala Pro Arg Ser Val Lys 50 55 60 Met Ala Asp Arg Arg Arg Arg Leu Gly Ala Ala Asp Val Asn His Gly 65 70 75 80 Gly Glu Glu Arg Arg Trp Ser Gly Tyr Thr Ser Ile Thr Glu Gly Arg 85 90 95 Ala Gly Trp Gln Ile Ile 100 29 187 PRT Japanese Macaque Herpesvirus 29 Met Ala Ala Ile Gln Gly Pro Pro Pro Leu Pro Glu Glu Glu Asn Glu 1 5 10 15 Asn Ser Leu Pro Asp Asp Val Tyr Ala Ile Glu Gly Ile Phe Leu Tyr 20 25 30 Cys Gly Leu Gly Gln Ala Glu Tyr Leu His His Pro Val Phe Ser Pro 35 40 45 Ile Lys Glu Phe Ile Ser Ser Phe Leu Lys Asp Ser Ala Arg Leu Tyr 50 55 60 Glu Arg Leu Leu Arg His Thr Asp Tyr Arg Ser Leu Arg Gly Leu Asn 65 70 75 80 Ala Ile Gly Gln Gly Met Leu His Ile Asn Thr Asp Gly Arg His Asn 85 90 95 Trp Gly Arg Ala Leu Ala Val Leu Gly Leu Gly Ala Tyr Val Val Asp 100 105 110 Lys Ile Arg Asp Asp Glu Arg Leu Leu Thr Phe Ala Ile Ala Val Leu 115 120 125 Pro Val Tyr Ala Tyr Glu Ala Leu Glu Ser Gln Trp Phe Arg Ser His 130 135 140 Gly Gly Trp Glu Gly Leu Arg Asn Tyr Cys Glu Arg Ile Leu Arg His 145 150 155 160 Arg Arg Asn Ala Arg Arg His Met Cys Tyr Gly Val Ala Ala Gly Leu 165 170 175 Leu Ala Leu Val Ala Leu Phe Ala Ile Arg Arg 180 185 30 536 PRT Japanese Macaque Herpesvirus 30 Met Thr Ser Val Tyr Val Gly Gly Tyr Val Asp Val Val Ser Leu Pro 1 5 10 15 Lys Ile Glu Lys Asp Leu Tyr Leu Glu Pro Ser Ile Val Ala Thr Leu 20 25 30 Leu Pro Tyr Thr Asn Pro Leu Pro Ile Asn Ile Glu His Val Pro Glu 35 40 45 Ala His Val Gly His Thr Leu Gly Leu Phe Gln Val Thr His Gly Ile 50 55 60 Phe Cys Leu Gly Lys Leu Thr Ser Pro Asp Phe Leu Ala Leu Ala Ser 65 70 75 80 Arg Leu Ala Gly Asp Ser Arg Ala Ala Gln Ile Gln Leu Asn Pro Met 85 90 95 Pro Arg Asp Pro Leu Leu Glu Met Leu His Thr Trp Leu Pro Glu Leu 100 105 110 Ser Leu Ser Ser Leu His Pro Glu Glu Leu Gln Asp Pro Asn His Pro 115 120 125 Pro Ala Phe Gln His Val Ser Leu Cys Ala Leu Gly Arg Arg Arg Gly 130 135 140 Ser Ile Ala Val Tyr Gly Pro Asp Pro Thr Trp Val Val Ser Lys Phe 145 150 155 160 Asp Ser Leu Thr Arg Asp Glu Ala Gly Lys Ile Thr Ser Lys Cys Leu 165 170 175 Asp Leu Cys Glu Arg Gln Val Thr Pro Pro Glu Phe Ala Ala Pro Leu 180 185 190 Glu Thr Leu Met Ala Lys Ala Ile Asp Ala Gly Phe Ile Arg Asp Arg 195 200 205 Thr Asp Leu Leu Lys Thr Asp Lys Gly Val Ala Arg Val Ala Arg Ser 210 215 220 Thr Tyr Leu Lys Ala Ser Gln Ser Pro Ser Ser Gln His Gly Gly Asn 225 230 235 240 Arg Asp Thr Gln Thr Met Ser Ala Leu Pro Asp Asp Asn Ile Thr Ile 245 250 255 Pro Lys Ser Thr Phe Leu Thr Met Val Gln Ser Ser Leu Asp His Met 260 265 270 Arg Asn Gln Gly Gln Arg Ala Tyr Val Ser Ala Pro Pro Ser Met Pro 275 280 285 Ala Thr Ala Ala Tyr Pro Ser Trp Ile Pro Pro Pro Glu Leu Thr Val 290 295 300 Pro Ser Tyr Ala Pro Pro Val Ala Pro Pro Phe Pro Phe Gln Ser Ala 305 310 315 320 Phe Ala Pro Gln Pro Ser Pro Tyr Ala Ala Thr Tyr Tyr Ser Pro Thr 325 330 335 Tyr Gly Tyr Ala Gln Ala Pro Ser Arg His Gln Lys Arg Lys Arg Asp 340 345 350 Val Glu Leu Ser Asp Glu Pro Val Phe Pro Gly Glu Glu Val Gly Ile 355 360 365 His Lys Asp Val Met Ala Leu Ser Lys Asn Ile Leu Asp Ile Gln Ala 370 375 380 Asp Leu Arg Asp Leu Lys Arg Ala Ala Ser Gln Thr Ser Gly Glu Lys 385 390 395 400 Asp Thr Asp Gln Arg Pro Gln Pro Pro Pro Val Gln Phe Ser Trp Pro 405 410 415 Gln Thr Tyr Ala Ser Ala Pro Tyr Leu Ala Tyr Gln Pro Gln Trp Tyr 420 425 430 Pro Gly Thr Asp Thr His Leu His Ala Ser Gln Pro Tyr Gln Ile Ala 435 440 445 Gln Gly Ile Gln Gln Thr Gln Pro Pro Pro Pro Gln Pro Ala Ser His 450 455 460 His Ala Gly Leu Ala Thr Gln Pro Val Ala Pro Ala Pro Ala Ala Gln 465 470 475 480 Glu Ser Ala Met Ser Asn Ala Val Pro Ser Ala Ser Ala Pro Arg Ala 485 490 495 Gly Ala Cys Pro Pro Leu Asp Ser Asp Cys Gly Gln Ser Ala Arg Ala 500 505 510 Pro Val Glu Ala Ser Val Gln Pro Ala Pro Val Ser Gln Ile Gln Lys 515 520 525 Met Phe Cys Glu Glu Leu Leu Lys 530 535 31 299 PRT Japanese Macaque Herpesvirus 31 Met Phe Ile Gly Arg Gly Phe Val Tyr Gly Ser Arg Val Ala Thr Ile 1 5 10 15 Glu Gly Ser Lys Tyr Arg Ser Phe Ser Ile Phe Gly Arg Leu Thr Thr 20 25 30 Ser Thr Tyr Pro Pro Thr Tyr Thr Glu Val Met Leu Gly Arg Cys Leu 35 40 45 Arg Glu Pro Lys Glu Met Ser Ala Gly Leu Arg Gly Leu Met Trp Arg 50 55 60 Val Ile Arg Cys Glu Asn Leu Asn Thr Phe Leu Pro Gly Glu Leu Arg 65 70 75 80 Phe Leu His Leu Val Leu Cys Glu Met Tyr Asn Tyr Gly Leu Asn Val 85 90 95 Tyr Leu Leu Lys Glu Ala Ile Ala Asn Thr Gly Thr Arg Asp Asp Ile 100 105 110 Val Leu Gly Arg Lys Val Pro Val Glu Phe Trp Lys Ile Ile Tyr Asp 115 120 125 Gly Leu Arg Glu Met Gly Val Ser Asp Ala Thr Leu Leu Ser Glu Thr 130 135 140 Lys Arg Gly Ala Leu Trp Leu Tyr Phe Asn Gly Arg Pro Cys Leu Leu 145 150 155 160 Lys Gly Leu Gly Asp Tyr Val Phe Cys Arg Leu Gly Leu Ser His Ser 165 170 175 Val Arg Val Val Pro Glu Asn Leu Thr Asp Gly Asn Tyr Leu Tyr Asn 180 185 190 Leu Gly Ser Val Ile Pro Cys Arg Leu Leu Val Ala Leu Ser Tyr Cys 195 200 205 Leu Ala Phe Trp Gly His Ala Asp His Glu Pro Trp Val Arg Leu Phe 210 215 220 Ala Gly Lys Ile Phe Ile Leu Tyr Leu Ile Ile Ser Gly His Ile Met 225 230 235 240 Pro Arg Lys Ser Ile Leu Glu Gln Val Gly Thr Ser Gly Tyr Gly Gly 245 250 255 Phe Val Glu Ala Val Cys Arg Asp Val Arg Ala Val His Gly Ile Pro 260 265 270 Ala Trp Asp Phe Ala Ala Ala Ala Pro Ala Leu Thr Ser Arg Gln Thr 275 280 285 Asp Tyr Leu Phe Ala Phe Asn Asn Ser Val Val 290 295 32 97 PRT Japanese Macaque Herpesvirus 32 Met Ser Pro Ala Ser Gly Ala Glu Leu Leu Leu Gly Val Leu Gly Ala 1 5 10 15 Arg Arg Pro Arg Ala Leu Gly Gln Val Val Arg Arg Gln Asp Phe Tyr 20 25 30 Thr Val Leu Asn Asn Ile Arg Pro His Tyr Ala Thr Lys Val Asn Leu 35 40 45 Arg Thr Gly Gly Asn Val Arg Val Arg Trp Leu Cys Arg Gly Cys Val 50 55 60 Ser Arg Arg Ser Arg Gly Pro Arg His Ser Gly Val Gly Phe Cys Gly 65 70 75 80 Ser Gly Ser Gly Val Asn Val Ser Thr Asp Gly Leu Pro Val Cys Val 85 90 95 Gln 33 547 PRT Japanese Macaque Herpesvirus 33 Met Arg Thr Ser Glu Lys Cys Cys Met Arg Tyr Pro Arg Lys Pro Ala 1 5 10 15 Arg Gln Ile Thr Ala Thr Phe Trp Ala Pro His Pro Asn Asn Val Leu 20 25 30 Phe Ile His Lys Pro Ser Leu Ile Glu Glu Arg Arg Asn Ala Phe Val 35 40 45 Met Arg Asn Gln Gln Leu Ala Leu Arg Val His Thr Leu Arg Lys Asn 50 55 60 Leu Leu Arg Leu Glu Leu Asp Asn Val Leu Gln Thr His Gln Arg Glu 65 70 75 80 Thr Glu Met Val Met Arg Asp Leu Asp Thr Ile Gln Asn Met Val Gly 85 90 95 Asp Leu Arg Ser Pro Thr Arg Glu Thr Ala Asp Thr Gln Thr Ser Ile 100 105 110 Asn Pro Arg Pro Lys Ile Ala Pro Gln Thr His Gly Asp Ala Phe Val 115 120 125 Val Thr Ile Ala Pro Gly Asp Pro Gly Phe Thr Val Asn Gln Asp Leu 130 135 140 Arg Leu Glu Leu Leu Pro Ser Leu Tyr Met Asn Gln Asn Gln Trp Leu 145 150 155 160 Pro Gln Tyr Gly Pro Trp Tyr Ser Ser Leu Thr Asp Asn Ala Met Gln 165 170 175 Arg Arg Val Phe Pro Arg Asp Leu Arg Gly Thr Thr Asn Phe Gln Asn 180 185 190 Ser Thr Ser Leu Lys Leu Met Ser Ala Val Ile Ser Thr Ala Ala Ser 195 200 205 Ile Thr Gln Asp Phe Tyr Ala Asp Val Arg Asn Val Ser Asp Thr Gln 210 215 220 Ala Ala Leu Cys Leu Leu Asn Gly Tyr Tyr Cys His Arg Thr Gly Thr 225 230 235 240 Pro Leu Pro Pro Thr Arg Asp Gly Leu Trp Asp Asn Leu Gly Thr Lys 245 250 255 Leu Ala Thr Leu Ile Ser His Leu Lys Gln Asn Thr Lys Gly Leu Gly 260 265 270 Phe Glu Phe Thr Tyr Ser Asn Pro Lys Gln Arg Ala Ser Leu Ala Pro 275 280 285 Leu Asn Lys Glu Thr Lys Tyr Ser Ala Asp Phe Phe Thr Asn His Val 290 295 300 Ile Tyr Ala Thr Leu Ala Gln Ser Gly Leu Leu Pro Gly Ser Lys Asn 305 310 315 320 Pro Gly Thr Gly Gln Pro Pro Gly Pro Asp Leu Val Tyr Ile Leu Ala 325 330 335 Thr Thr Leu Phe Ser Glu Asp Val Pro Pro Phe Gln Ala Tyr Gln Trp 340 345 350 Asn Leu Arg Ala Gly Leu Ser Ala Leu Gly Cys Leu Val Leu Val Tyr 355 360 365 Val Leu Leu Glu Leu Ala Gln Ile Thr Pro Arg Ser Pro His Arg Arg 370 375 380 Leu Asn Leu Ala Ser Leu Leu Gly Gly Arg Phe Ser Lys Val Glu Asp 385 390 395 400 Pro Ser Gly Ser Lys Gln Tyr Leu Lys Lys Gly Gln Leu Phe Asp Phe 405 410 415 Leu Thr Glu Asn Tyr Ile Ser Pro Leu Leu Ser Arg Ala Pro Asp Ala 420 425 430 Pro Thr Ser Phe Leu Phe Pro Gly Ala Tyr Leu Thr Ala Leu Glu Ala 435 440 445 Lys Ala Ile Ser His Leu Lys His Thr Arg Pro Phe Val Asn Leu Thr 450 455 460 Gly Ser Arg Phe Asn Glu Ile Phe Asp Ile Leu Asn Gln Lys Leu Thr 465 470 475 480 Phe Arg Asp Ala Gly Ser Leu Ile Gln Ala Gln Thr Ser Leu Arg Leu 485 490 495 Thr Ala Glu Glu Gly Leu Ala Ala Ile Leu Ser His Pro Ser Pro Pro 500 505 510 Gly Leu Thr His Glu Ile Met Lys Ser Gln Phe Gly Val Tyr Asp Asp 515 520 525 Tyr Asp Lys Val Tyr Phe Leu Val Leu Gly Tyr Leu Pro Val Ala Thr 530 535 540 Ser Val Val 545 34 350 PRT Japanese Macaque Herpesvirus 34 Met Thr Val Ala Asn Gln Cys Lys His Ala Ala Thr Leu Glu Ala Leu 1 5 10 15 Pro Ala Ser Arg Lys Arg Ala Gly Ile Arg Ala His Leu Ala Val Tyr 20 25 30 Arg Arg Leu Ile Lys His Arg Ser Leu Asp Asp Ile Leu Lys Phe Leu 35 40 45 Ser Ile Arg Pro Thr Arg Glu Ala Thr Lys Asp Val Lys Phe Arg Ile 50 55 60 Phe Phe Glu Val Thr Leu Gly Arg Arg Ile Ala Asp Cys Val Leu Thr 65 70 75 80 Val Asp Ser Glu His Gln Lys Thr Cys Tyr Val Ile Glu Leu Lys Thr 85 90 95 Cys Leu Ser Ala Ala Val Phe Pro Gly Asn Ala Ile Lys Ile Ser Gln 100 105 110 Arg Trp Gln Gly Leu His Gln Leu Thr Asp Ser Val Ala Tyr Ile Gly 115 120 125 Arg Ala Ala Pro Arg Gly His Glu Asn Trp Ser Val Arg Pro Trp Leu 130 135 140 Leu Phe Lys Asn Gln Lys Thr Leu Lys Thr Ile His Thr Glu Ser Ser 145 150 155 160 Ala Phe Pro Pro Thr Phe Ile Asn Thr Thr Ser Val Ala Leu Asn Gly 165 170 175 Phe Phe Ser Gln Trp Glu Asp Ala His Val Arg Lys Met Leu Tyr Glu 180 185 190 Ile Ser Thr Lys Thr Ser Ala Ala Asn Tyr Arg Asn Phe Leu Gly Pro 195 200 205 Thr Ser Lys Gln Arg Ser Val His Ser Gln Thr Ile Ala Asp Arg Arg 210 215 220 Lys Lys Lys Arg Val Cys Asp Ala Lys Ser Thr Ala Gly Ala Lys Gly 225 230 235 240 Ser His Ala Ala Lys Lys Pro Ala Pro Ser Arg Ala Arg Gln Arg Ala 245 250 255 Ala Asp Ala Pro Thr Gly Asn Arg Asn Gly His Ala Arg Pro Arg His 260 265 270 Asn Ser Lys His Gly Arg Gly Ser Ala Val Pro Asp Gln Gly Asn Arg 275 280 285 Arg Tyr Pro Asn Val Asn Lys Pro Thr Thr Gln Asn Arg Pro Ser Asp 290 295 300 Thr Trp Arg Arg Val Cys Cys His Asp Ser Pro Arg Arg Pro Gly Leu 305 310 315 320 His Gly Lys Pro Gly Ser Pro Ser Gly Ala Pro Ala Gln Pro Val His 325 330 335 Glu Pro Lys Pro Met Ala Ala Thr Ile Arg Ser Val Val Gln 340 345 350 35 556 PRT Japanese Macaque Herpesvirus 35 Met Ala Glu Gly Gly Ser Gly Phe Gly Asp Glu Leu Val Arg Gln Met 1 5 10 15 Arg Asp Arg Lys Pro Arg Trp Asp Glu Ser Ser Asp Asp Thr Asp Asp 20 25 30 Val Asp Thr Glu Ser Thr Asp Leu Glu Tyr Asp Asp Val Phe Pro Val 35 40 45 Val Asp Thr His Gly Leu Thr Ser Pro Gly Ser Gln Asn Tyr Asp Val 50 55 60 Pro Thr Ser Pro Ser Gly Thr Pro Trp Glu Leu Leu His Pro Asp Ala 65 70 75 80 Leu Tyr Ala Gln Pro Arg Cys Pro Pro Lys Arg Ala Ala Val Pro Gly 85 90 95 Gly Gly Ala Arg Pro Lys Val Ser Ala Phe Ser Ala Arg Leu Gln Tyr 100 105 110 Val Gly Arg Gln Ser Phe Gly Asp Arg Glu Thr Arg Gln Leu Thr Gly 115 120 125 Ala Gln Phe Ser Ser Glu Ser Glu His Glu Tyr Ala Glu Ile Pro Glu 130 135 140 Arg Thr Thr Arg Pro Val Glu Ser Gly Asp Lys Arg His Phe Thr Ser 145 150 155 160 Gly Arg Arg Gly Gly Ile Ser Gly Pro Ser Ser Ser Lys Pro Ser Asn 165 170 175 Gly Ala Gly Leu Thr Arg Lys Thr Lys Thr Ser Leu Ser Val Ser Leu 180 185 190 Lys Asn Leu Leu Arg Ile Lys Asp Asp Asp Val Lys Val Asp Val Pro 195 200 205 Arg Pro Val Thr Val Pro Val His Leu Met Gln Pro His Pro Met Thr 210 215 220 Glu Tyr Arg Asn Ala Phe Leu Ile Tyr Leu Glu Gly Val Met Gly Val 225 230 235 240 Gly Lys Thr Thr Leu Leu Asn Ser Met Thr Gly Met Val Pro Gln Glu 245 250 255 Asn Val Leu Ser Cys Pro Glu Pro Met Lys Phe Trp Thr Cys Val Tyr 260 265 270 Ser Asn Cys Leu Lys Glu Gln Arg Ser Ile Val Lys Gln Gly Thr His 275 280 285 Gly Lys Ser Ile Thr Ser Ala Arg Val Tyr Ala Cys Gln Ser Lys Phe 290 295 300 Ala Leu Pro Phe Arg Ala Thr Ala Ala Gly Ile Gly Arg Asn Leu Gln 305 310 315 320 Pro Trp Leu Val Gly Asn Gly Ser Thr Lys Pro Ala Asn Trp Ile Val 325 330 335 Phe Asp Arg His Leu Leu Ser Ala Thr Val Val Phe Pro Leu Val His 340 345 350 Val Lys Tyr Asn Arg Leu Thr Pro Asp His Leu Phe Gln Ile Leu Ser 355 360 365 Leu Phe Ser Ala His Asp Gly Asp Val Val Val Leu Leu Thr Leu Asn 370 375 380 Ser Ser Glu Ala His Arg Arg Ile Gln Ser Arg Gly Arg Lys Glu Glu 385 390 395 400 Lys Gly Ile Thr Gln Asn Tyr Leu Arg Gln Val Ala Trp Ala Tyr His 405 410 415 Ala Val Phe Cys Thr Trp Val Met Met Gln Tyr Leu Thr Pro Glu Gln 420 425 430 Met Val Gln Leu Cys Val Gln Thr Val Ser Ile Glu Asp Ile Cys Asn 435 440 445 Met Asn Ser Arg Leu Thr His Arg Phe Leu Thr Leu Thr Lys Leu His 450 455 460 Glu Gln Ser Met Ile Pro Met Val Val Glu Met Leu Ala Ala Val Lys 465 470 475 480 Glu His Val Thr Leu Met Glu Val Cys Leu Gly Leu Phe Lys Glu Leu 485 490 495 Arg Lys Leu Gln Ile Leu Ile Val Asp Ala Gly Glu His Leu Asp Asp 500 505 510 Thr Cys Gly Leu Trp Gly Asn Ile Tyr Gly Gln Val Met Ser Asn Glu 515 520 525 Ala Ile Lys Pro Arg Ala Val Asn Trp Pro Ala Leu Glu Ser Tyr Ile 530 535 540 Gln Thr Leu Thr Ser Leu Glu Ser Asn Ala Ala Asn 545 550 555 36 118 PRT Japanese Macaque Herpesvirus 36 Met Thr Tyr Pro Arg Leu Arg Pro Glu Arg Arg Gly Asn Tyr Cys Thr 1 5 10 15 Arg Thr Leu Cys Met Arg Ser Arg Gly Ala His Leu Lys Gly Arg Pro 20 25 30 Cys Arg Ala Val Val Arg Gly Pro Arg Cys Pro Arg Ser Arg Leu Asp 35 40 45 Phe Asn Met Leu Asp Asp Arg Val Leu Gly Ile Glu Arg Arg Gly Ser 50 55 60 Leu Pro Gly Pro Ser Phe Leu Pro Arg Ala Ser Thr Asn Met Arg Lys 65 70 75 80 Tyr Arg Ser Val Leu His Ala Arg Leu Lys Ala Gly Thr Arg Asp Ile 85 90 95 Leu Pro Leu Gly Val Gly Val Glu Phe Arg Asp Pro Arg Arg Gln Asn 100 105 110 Leu Val Thr Val Arg Gly 115 37 82 PRT Japanese Macaque Herpesvirus 37 Met Ser Leu Val Pro Ala Phe Asn Arg Ala Cys Ser Thr Leu Arg Tyr 1 5 10 15 Phe Arg Ile Phe Val Leu Ala Leu Gly Arg Lys Leu Gly Pro Gly Lys 20 25 30 Leu Pro Arg Leu Ser Ile Pro Lys Thr Leu Ser Ser Asn Ile Leu Lys 35 40 45 Ser Ser Arg Glu Arg Gly His Leu Gly Pro Arg Thr Thr Ala Arg His 50 55 60 Gly Arg Pro Phe Arg Trp Ala Pro Arg Leu Arg Ile Gln Ser Val Arg 65 70 75 80 Val Gln 38 109 PRT Japanese Macaque Herpesvirus 38 Met Phe Asn Phe Lys Ile Pro Phe Leu Phe Cys Asn Val Ser Cys Asn 1 5 10 15 Val Ser Arg Ile Phe Glu Leu Ala Gln Ala Ser Cys Ile Thr Arg Glu 20 25 30 Val Asn Thr Ser Leu Thr Phe Phe Gln Leu Ile Arg Tyr Arg Val Leu 35 40 45 Leu Asn Ser Ser Ser Thr Val Asp Ile Ser Leu Leu Thr Gly Val Val 50 55 60 Val Ala Gly Val Lys Arg Thr Ile Ser Ser Pro Gly Thr Phe Ser Ser 65 70 75 80 Leu Tyr Ser Tyr Pro Leu Ile Thr Glu Asn Val Ile Thr Asn Lys His 85 90 95 Lys Pro Trp Leu Ile Gly Cys Ile Ala Phe Gln Ala Gly 100 105 39 726 PRT Japanese Macaque Herpesvirus 39 Met Gln Pro Ile Asn His Gly Leu Cys Leu Leu Val Ile Thr Phe Ser 1 5 10 15 Val Ile Asn Gly Tyr Glu Tyr Asn Glu Glu Asn Val Pro Gly Leu Glu 20 25 30 Ile Val Leu Phe Thr Pro Ala Thr Thr Thr Pro Val Lys Ser Asp Ile 35 40 45 Ser Thr Val Glu Leu Glu Phe Asn Arg Thr Arg Tyr Arg Ile Asn Trp 50 55 60 Lys Asn Val Ser Glu Val Leu Thr Ser Arg Val Ile Gln Asp Ala Trp 65 70 75 80 Ala Ser Ser Lys Ile Leu Glu Thr Leu Gln Glu Thr Leu Gln Lys Arg 85 90 95 Lys Gly Ile Leu Lys Leu Asn Met Ala Tyr Val Ser Asn Lys Glu Ile 100 105 110 Asn Phe Cys Lys Ser Phe Ser Ser Ser Glu Ile Ile Asn Ile Thr Ser 115 120 125 Asp Phe Asn Tyr Ser Ser Leu Pro Gly Phe Leu Gly Ser Phe Asp Val 130 135 140 Ile Asn His Glu Leu Thr His Gly Val Leu Val Ser Lys Arg Glu Leu 145 150 155 160 Phe Thr Asn Ala Leu Asp Ile Met Gly Leu Phe Tyr Ala Ile Lys Leu 165 170 175 Asn Ala Glu Thr Phe Lys Ile Thr Phe Asp Glu Ser Lys Val Ile Ile 180 185 190 Ser Gly Ile Met Thr Ala Asp Trp Ile Leu Val Ser Ile Ala Asn Ser 195 200 205 Ser Ser Glu Val Asn Gly Gln Cys Val Ala Leu Leu Phe Gly Asp Pro 210 215 220 Glu Lys Phe Pro Pro Leu Lys Gly Tyr Val Ser Tyr Arg Asp Leu Val 225 230 235 240 Val Val Arg Asn Asp Asn Tyr Ala Ile Ala Val Ile Ala Pro Met Ser 245 250 255 His Gly Thr Met Gly Leu Asn Phe Leu Pro Gln Asn Leu Thr Asp Ile 260 265 270 Phe Phe Ser Ile Leu Asn Ser Pro Leu Lys Val Ile Asn Tyr Leu Lys 275 280 285 Gly Lys Leu Phe Glu Leu Glu Ser Lys Gly Ala Cys Gln Asn Pro Ser 290 295 300 Asn Glu Gln Asn Ile Leu Ser Leu Phe Phe Glu Val Thr Ala Ile His 305 310 315 320 Phe Leu Tyr Val Arg Asn Leu Asn Lys Glu Glu Pro Val Asn Val Gly 325 330 335 Cys Val Val Lys His Val Ala Ala Leu Lys Ser Leu Glu Arg Leu Phe 340 345 350 Lys Leu Cys Phe Pro Ala Phe Glu Leu His Ser Leu Asn Leu Trp Thr 355 360 365 Leu Ser His Leu Ala Ala Ser Gln Ile Ala Asn Leu Pro Pro Asn Asn 370 375 380 Val Met Ser Leu Thr Met Asp Glu Gln Glu Val Val Phe Ser Met Phe 385 390 395 400 Lys Leu Ala Asp Asn Asn Asn Val Asn Glu Ile Ile Leu Asn Glu Ile 405 410 415 Ile Asn Ile Ser Asp Gln Met Tyr Thr Met Tyr Ser Asp Ile Tyr Gln 420 425 430 Leu Ser Asn Thr Tyr Arg Gln Thr Val Met Asp Ile Tyr Glu Val Leu 435 440 445 Thr Thr Val Ser Leu Thr Asn Val Gly Ala Arg Ala Val Tyr Pro Tyr 450 455 460 Ile Leu Phe Thr Ser Met Cys Asn Asn Val Glu Ile Ser Tyr Met Ile 465 470 475 480 Asn Gln Ile Ser Lys Pro Asp Asp Ile Thr Ile Phe Arg Val Phe Ser 485 490 495 Pro Cys Phe Leu Ser Leu Arg Phe Asp Leu Asp Glu Asn Lys Leu Arg 500 505 510 Ser Asp Ala Pro Gln Thr Ser Lys Arg Thr Gly Ser Glu Leu Ala Gln 515 520 525 Gly Ala Ser Gly Phe Trp Arg Leu Leu His Ala Phe His Ala Thr Arg 530 535 540 Ile Asn Glu Phe Ser Val Ile Asn Cys Thr Arg Leu Ala Trp Lys Gln 545 550 555 560 Val Thr Ala Leu Met Pro Leu Thr Asn Ile Thr Tyr Val Ile Ser Ser 565 570 575 Val Arg Pro Asp His Ala Arg Val Tyr Glu Val Ser Glu Val Phe Leu 580 585 590 Asn Ser Ala Met Phe Val Ser Ala Val Tyr Pro Asn Cys Ser His Phe 595 600 605 Thr Pro Pro Gly Thr Ala Leu His Ile Pro Ile Leu Tyr Asn Phe Ser 610 615 620 Ala Pro Arg Ile Gly Cys Pro Leu Cys Asp Ser Ile Val Leu Ser Tyr 625 630 635 640 Asp Glu Asn Gln Gly Leu Gln Thr Met Met Tyr Val Ser Asn Pro Gln 645 650 655 Val Gln Ala Asn Leu Phe Ser Pro Tyr Ser Pro Phe Phe Asp Asn Asp 660 665 670 Asn Phe His Ile His Tyr Leu Trp Leu Met Asn Asn Gly Thr Val Val 675 680 685 Glu Ile Arg Gly Leu Tyr Arg Arg His Ala Leu Ser Ala Ile Ala Phe 690 695 700 Val Phe Ala Phe Ile Gly Thr Met Ser Ala Leu Tyr Phe Leu Phe Lys 705 710 715 720 Leu Phe Ser Ile Leu Ala 725 40 99 PRT Japanese Macaque Herpesvirus 40 Met Phe Ile Ile Ser Phe Lys Met Ile Ser Phe Thr Leu Leu Leu Ser 1 5 10 15 Ala Ser Leu Asn Ile Glu Asn Thr Thr Ser Cys Ser Ser Ile Val Asn 20 25 30 Asp Ile Thr Leu Phe Gly Gly Lys Leu Ala Ile Cys Asp Ala Ala Arg 35 40 45 Cys Asp Asn Val His Lys Leu Ser Glu Cys Asn Ser Asn Ala Gly Lys 50 55 60 His Asn Leu Asn Asn Leu Ser Lys Leu Phe Lys Ala Ala Thr Cys Phe 65 70 75 80 Thr Thr His Pro Thr Phe Thr Gly Ser Ser Leu Phe Lys Phe Leu Thr 85 90 95 Tyr Lys Lys 41 187 PRT Japanese Macaque Herpesvirus 41 Met Gly Ser Arg Gln Pro Gln Ile Gly Glu Ser Pro Ile Thr Ala Phe 1 5 10 15 Asn Thr Val Thr Ile Met Gln Arg Ala Asn Asn Ser Ile Met Phe Leu 20 25 30 Pro Asn Leu Lys Leu Lys Pro Ile Gln His Leu Phe Leu Lys His Val 35 40 45 Leu Leu Gln Arg Leu Gly Leu Glu Asn Ile Leu Phe His Phe Lys Met 50 55 60 Leu Tyr Ala Asn Thr Cys Lys Ala Ala Ala Pro Tyr Gln Arg Glu Tyr 65 70 75 80 Phe Glu Ser Met Leu Ser Arg Val Lys Gln Arg Leu Glu Asp Met Val 85 90 95 Phe Cys Leu Asn Ser Ile Glu Ser His Asn Phe Gln Lys Asp Phe Lys 100 105 110 Val Thr Ser Arg Ala Pro Gln Gln Leu Leu Thr Ala Thr Asp Lys Tyr 115 120 125 Phe Leu Met Phe Pro Pro Gln Asn Arg Asp Leu Ala Ile Gln Val Gly 130 135 140 Ala Glu Val Ile Glu Ser Ile Cys Asp Gly Thr Pro Leu Phe Glu Val 145 150 155 160 Leu Ala Asn Leu Asn Pro Arg Val Thr Ile Gln Lys Glu Thr Gly Asn 165 170 175 Asn Leu Leu Lys Phe Tyr Ala Leu Leu Thr Val 180 185 42 103 PRT Japanese Macaque Herpesvirus 42 Met Ile Val Thr Val Leu Asn Ala Val Ile Gly Leu Ser Pro Ile Cys 1 5 10 15 Gly Trp Arg Glu Pro Met Ala Lys Asn Met Ser Ala Ser Lys Gln Ser 20 25 30 Asp Cys Thr Ser Glu Ser Leu Val Ala Gly Gly Cys Leu Arg Met Asp 35 40 45 Arg Ser Phe Leu Ser Ser Asp Val Lys Gly Ala Leu His Lys Val Gly 50 55 60 Gly Ala Phe Gly Ser Tyr Ser Cys Val Val Phe Ala Ser Ser Phe Met 65 70 75 80 Val Ile Cys Leu Leu Phe Val Arg Val Thr Gly Gly Val Leu Thr Val 85 90 95 Thr Trp Thr Glu Asn Gly Leu 100 43 128 PRT Japanese Macaque Herpesvirus 43 Met Ile Lys Ile Pro Asp Leu Lys Ala Arg Leu Val Gly Gly Ala Val 1 5 10 15 Gln Leu Ser Asn Gly Glu Tyr Val Cys His Val Val Tyr Ser Ser Ala 20 25 30 Leu Ala Ala Met Val Gly Leu Pro Gly Pro Ala Val Pro Leu Pro Leu 35 40 45 Leu Phe Lys Lys Phe Gly Thr Ile Tyr Ser Asn Met Met Pro Leu Tyr 50 55 60 Ala Pro Lys Arg Pro Glu Leu Ser Met Leu Arg Ile Met Val Ser Pro 65 70 75 80 His Pro Tyr Ala Leu Asn Ser Cys Leu Cys Val Gly Thr Asp Glu Gly 85 90 95 Glu Arg Gly Val Ser Leu Phe Arg Asp Pro Val Ile Arg Ser Ser Asp 100 105 110 Phe Asp Asp Thr Pro Ile Thr Val Arg Leu Lys Ile Ser Asp Arg Glu 115 120 125 44 733 PRT Japanese Macaque Herpesvirus 44 Met Met Leu Leu Gln Gly Pro Val Leu Leu Pro Ala Cys Pro Ala Thr 1 5 10 15 Ala Thr Ala Asp Thr Pro Ser Pro Ala Asn Ser Asp Phe Lys Thr Gln 20 25 30 Leu Ala Ile Phe Cys Cys Leu Ala Thr Asn Asn Glu Ile Leu Glu Asn 35 40 45 Val Ser Leu Glu Val Leu Asp Arg Ala Met Glu Thr Glu Thr Thr Phe 50 55 60 Tyr Ala Cys Arg Ala Leu Arg Arg Leu Val Leu Gly Glu Gly Leu Tyr 65 70 75 80 Pro Phe Ile His Arg Gln Gly Gly Ile Val Gly Lys Thr Gly Asn Glu 85 90 95 Tyr Ala Gly Pro Gly Leu Ile Ile Asp Asp Ala Ile Gly Cys Thr Phe 100 105 110 Ser His Ile Glu Thr His Thr Phe Leu Pro Thr Val Phe Thr Tyr Glu 115 120 125 Leu Ser Asp Thr Val Trp Val Gln Arg Asp Glu Arg Ile Leu Arg Ser 130 135 140 Leu Tyr Cys Ser Pro Leu Met Val Cys Gly Val Asn Tyr Gln Ser Met 145 150 155 160 Phe Arg Ile Leu Cys Arg Tyr Leu Gln Ile Trp Glu Phe Glu Glu Cys 165 170 175 Phe Ala Ala Phe Thr Arg Thr Leu Pro Glu His Leu Ile Gly Thr Cys 180 185 190 Tyr Gln Asn Tyr Phe Lys Leu Leu Glu Pro Phe Lys Thr Leu Thr Leu 195 200 205 Ala Arg Cys Pro Pro Pro Cys Ala Lys Leu His Leu Asn Tyr Leu Lys 210 215 220 Phe Asn Ile Leu Gly Phe Thr Ser Asp Trp Ile Ser His Pro Glu Leu 225 230 235 240 His Arg Val Gln Thr Val Ile Ile Tyr Asn Ile Glu Ser Asn Pro Val 245 250 255 Leu Leu Lys Asn Leu Ser Lys Gln Asn Lys Phe Gln Asp Ile Arg Val 260 265 270 Ala Ser Glu Leu Ile Ile Asp Tyr Gln Asn Ile Val Asn Gln Ser Leu 275 280 285 Gly Val Asn Leu Gln Val Lys Ile Asn Lys Lys Asp Pro Gly Lys Lys 290 295 300 Pro Tyr Lys Val Val Val Val Thr Pro Lys Ser Thr Tyr Tyr Leu Thr 305 310 315 320 Phe Pro Pro Glu Val Pro Ile Phe Arg Val Ala Met Cys Met Ser Val 325 330 335 Ala Glu His Val Cys His Ser Cys Asp Arg Leu Tyr Pro Asn Thr Glu 340 345 350 Phe Leu Gly Pro Gly Glu Thr Pro Arg Val Leu Glu Ala Met Phe Ser 355 360 365 Arg Ile Gln Tyr Ala Pro Lys Asp Arg Asp His Asn Phe Ile Phe Asp 370 375 380 Ala Asn Gln Asn Pro Asp Arg His Lys Gln Val His His Asp His Gln 385 390 395 400 Thr Glu Pro Leu Pro Asp Met Phe Asp Pro Val Lys His Leu Ser Leu 405 410 415 His Asn Phe Lys Ile Ser Val Phe Asn Thr Asn Met Val Ile Asn Thr 420 425 430 Lys Ile Thr Cys Arg Ser Leu Thr Gly Thr Phe Glu Ser Ile Ile Asp 435 440 445 Ile Pro Arg Leu Thr Asn Asn Phe Val Met Lys Lys Phe Ser Val Lys 450 455 460 Glu Pro Ser Phe Thr Val Ser Val Phe Tyr Ser Asp Asn Leu Cys Asn 465 470 475 480 Gly Ala Ala Ile Asn Val Asn Ile Ser Gly Asp Met Leu His Phe Met 485 490 495 Phe Ala Met Gly Asn Leu Arg Cys Phe Leu Pro Val Lys His Ile Phe 500 505 510 Pro Val Ser Ile Ala Asn Trp Asn Ser Thr Leu Asp Leu His Gly Leu 515 520 525 Glu Asn Gln Tyr Ile Val Arg Arg Gly Arg Arg Asp Val Phe Trp Thr 530 535 540 Thr Asn Phe Pro Ser Val Val Ser Ser Lys Asp Gly Cys Asn Val Ser 545 550 555 560 Trp Phe Lys Ala Ala Thr Ala Thr Ile Ser Lys Ile Tyr Gly Arg Pro 565 570 575 Leu Leu Lys Lys Leu Ser Asp Glu Leu Asp Pro Ile Leu Ser Val Pro 580 585 590 Tyr Ala Arg Ile Asp Gln Val Lys Asn Thr Ile Phe Thr Thr Leu Glu 595 600 605 Thr Arg Asn Lys Ala Gln Ile Gln Thr Leu His Lys Arg Phe Ile Glu 610 615 620 Cys Leu Val Glu Cys Cys Ser Phe Leu Arg Leu Asp Leu Gly Ala Leu 625 630 635 640 Asn Arg Ala Ala Arg Leu Gly Ala Phe Asp Phe Ser Lys Arg Ile Ile 645 650 655 Ser His Thr Lys Ser Lys His Glu Cys Ala Ile Leu Gly Tyr Lys Lys 660 665 670 Cys Asn Leu Ile Pro Lys Ile Tyr Val Arg Ser Lys Lys Ile Arg Leu 675 680 685 Asp Glu Leu Gly Arg Asn Ala Asn Phe Met Ser Phe Ile Ala Thr Thr 690 695 700 Gly His Ala Phe Ser Asn Leu Lys Pro Gln Val Ile Arg His Thr Ile 705 710 715 720 Arg Arg Leu Gly Leu His Trp Arg His Lys Ala Lys Ile 725 730 45 88 PRT Japanese Macaque Herpesvirus 45 Met Tyr Ile Phe Pro His Arg Asn Ala Tyr Val Phe Thr His Arg Leu 1 5 10 15 His Leu Arg Thr Val Arg His Gly Leu Gly Ser Thr Arg Arg Thr Asn 20 25 30 Pro Thr Val Pro Val Leu Phe Ala Ile Asn Gly Met Trp Arg Lys Leu 35 40 45 Ser Lys His Val Ser Asn Ser Leu Ser Leu Pro Ser Asn Met Gly Ile 50 55 60 Arg Gly Met Leu Cys Arg Leu His Ala Tyr Thr Ala Gly Thr Ser Asp 65 70 75 80 Arg His Val Leu Ser Glu Leu Leu 85 46 1378 PRT Japanese Macaque Herpesvirus 46 Met Glu Ala Ala Leu Glu Val Arg Pro Phe Pro Tyr Met Ala Thr Glu 1 5 10 15 Ala Asn Leu Leu Arg Gln Met Lys Glu Ser Ala Ala Ser Gly Leu Phe 20 25 30 Lys Ser Phe Gln Leu Leu Leu Gly Lys Asp Ala Arg Glu Gly Gly Val 35 40 45 Gln Phe Glu Gly Leu Leu Gly Val Tyr Thr Asn Val Ile Gln Phe Val 50 55 60 Lys Phe Leu Glu Thr Ser Leu Ala Val Ala Cys Val Asn Thr Glu Phe 65 70 75 80 Lys Asp Leu Lys Arg Met Thr Asp Gly Lys Ile Gln Phe Lys Val Ser 85 90 95 Val Pro Thr Ile Ala Tyr Gly Asp Gly Arg Arg Pro Thr Lys Gln Lys 100 105 110 Gln Tyr Ile Ile Met Lys Ala Cys Asn Lys His His Ile Gly Ala Glu 115 120 125 Ile Glu Leu Ser Thr Asp Asp Ile Glu Leu Leu Phe Ile Asp Arg Glu 130 135 140 Thr Pro Leu Asp Tyr Thr Glu Tyr Ala Gly Ala Val Lys Thr Ile Thr 145 150 155 160 Ala Ser Leu Gln Phe Gly Val Asp Ala Leu Glu Arg Gly Leu Val Asp 165 170 175 Thr Val Leu Asn Val Lys Leu Arg Ser Ala Pro Pro Met Phe Ile Leu 180 185 190 Lys Thr Leu Ser Asp Pro Val Tyr Thr Glu Arg Gly Leu Lys Lys Ala 195 200 205 Val Lys Ser Asp Met Val Ser Met Phe Lys Ser Tyr Leu Met Asp Asn 210 215 220 Ser Phe Phe Leu Asp Lys Ser Asp Ile Ala Val Lys Gly Lys Gln Tyr 225 230 235 240 Val Leu Ser Val Leu Ser Asp Met Val Gly Ala Val Cys His Glu Thr 245 250 255 Val Phe Lys Gly Thr Asn Thr Tyr Leu Ser Ala Ser Gly Glu Pro Ile 260 265 270 Ala Gly Val Met Glu Thr Thr Glu Asn Val Met Arg Lys Leu Leu Asn 275 280 285 Met Leu Gly Gln Val Asp Gly Gly Met Ser Gly Pro Ala Ser Tyr Ala 290 295 300 Asn Tyr Val Val Arg Gly Glu Asn Leu Val Thr Ala Val Thr Tyr Gly 305 310 315 320 Arg Val Met Arg Thr Phe Asp Gln Phe Met Lys Arg Ile Val Asp Arg 325 330 335 Pro Asn Ala Gln Pro Asn Val Asp Asp Asp Arg Asp Ala Val Ala Asp 340 345 350 Gly Gln Asp Ser Leu Ala Lys Thr Pro Ile Ala Ala Ala Val Ile Gln 355 360 365 Ile Gly Asp Lys Leu Val Ala Leu Glu Ser Leu Gln Arg Met Tyr Asn 370 375 380 Glu Thr Gln Phe Pro Phe Pro Leu Asn Arg Arg Met His Tyr Thr Tyr 385 390 395 400 Phe Phe Pro Ile Gly Leu His Met Pro Arg Pro Gln Tyr Ser Thr Ser 405 410 415 Ala Thr Ile Lys Gly Val Glu Asn Pro Ala Glu Gln Ser Val Glu Thr 420 425 430 Trp Ile Val Asn Lys Asn Asn Val Leu Leu Ser Phe Asn Tyr Gln Asn 435 440 445 Ala Leu Lys Ser Ile Cys His Pro Arg Met His Asn Pro Ile Pro Cys 450 455 460 Gly Gln Ala Leu Gly Gln Ala Phe Pro Asp Pro Gly His Val His Arg 465 470 475 480 Tyr Gly Gln Lys Ser Glu His Pro Pro Asn Met Asn Leu Tyr Gly Leu 485 490 495 Val Tyr Asn Tyr Tyr Gln Gly Lys Asn Val Ala His Val Pro Asp Ile 500 505 510 Ala Leu Lys Ala Thr Met Thr Thr Asp Glu Leu Leu His Pro Thr Ser 515 520 525 His Glu Thr Leu Arg Leu Glu Val His Pro Met Phe Asp Phe Phe Val 530 535 540 His Gln Gln Pro Gly Ala Gln Ala Ala Tyr Arg Ala Thr His Arg Thr 545 550 555 560 Met Val Gly Asn Ile Pro Gln Pro Leu Ala Pro Asn Glu Phe Gln Asn 565 570 575 Ser Arg Gly Leu Gln Phe Asp Arg Ala Ala Ala Val Ala His Val Leu 580 585 590 Asp Gln Ser Thr Met Glu Ile Ile Gln Asp Thr Ala Phe Asp Thr Ser 595 600 605 Tyr Pro Leu Leu Cys Tyr Val Ile Glu Cys Leu Val His Gly Gln Glu 610 615 620 Asp Lys Phe Leu Ile Asn Ser Pro Leu Ile Ala Leu Thr Ile Glu Thr 625 630 635 640 Tyr Trp Asn Asn Ala Gly Lys Leu Ala Phe Ile Asn Ser Phe Pro Met 645 650 655 Leu Arg Phe Ile Cys Val His Leu Gly Asn Gly Ser Ile Ser Lys Asp 660 665 670 Val Tyr Ala His Tyr Arg Lys Val Phe Gly Glu Leu Val Val Leu Gln 675 680 685 Gln Ala Leu Ser Lys Ile Ala Gly His Glu Val Val Gly Arg Arg Pro 690 695 700 Ala Ser Glu Leu Ile Asn Cys Leu Gln Asp Pro Asn Leu Leu Pro Pro 705 710 715 720 Phe Ala Tyr Asn Asp Val Phe Thr Asn Leu Leu Arg Gln Ser Ser Arg 725 730 735 His Pro Met Val Leu Ile Gly Asp Glu Gly Tyr Glu Thr Glu Asn Asp 740 745 750 Arg Asp Thr Tyr Ile Asn Val Arg Gly Lys Met Glu Asp Leu Val Gly 755 760 765 Asp Met Val Asn Ile Tyr Glu Thr Arg Asn Asn Ala Asp His Asp Gly 770 775 780 Arg His Val Leu Asp Val Gly Pro Phe Asn Glu Asn Glu Gln His Met 785 790 795 800 Ala Val Leu Glu Lys Leu Phe Tyr Tyr Val Val Leu Pro Ala Cys Ala 805 810 815 Asn Gly His Val Cys Gly Met Gly Val Asp Phe Asp Asn Val Ala Leu 820 825 830 Ala Leu Thr Tyr Asn Gly Pro Val Phe Ala Asp Val Val Asn Pro Asp 835 840 845 Asp Glu Ile Leu Asp His Leu Glu Asn Gly Thr Leu Arg Glu Met Leu 850 855 860 Glu Ala Ser Asp Ile His Pro Thr Val Asp Met Ile Arg Thr Leu Cys 865 870 875 880 Thr Ser Phe Leu Thr Cys Pro Phe Val Thr Gln Ala Ser Arg Val Val 885 890 895 Thr Gln Arg Asp Pro Ala Gln Leu Leu Thr Thr His Asp Asp Gly Arg 900 905 910 Tyr Val Ser Gln Thr Val Leu Val Asn Gly Phe Ala Ala Phe Ala Ile 915 920 925 Ala Asp Arg Ser Arg Asp Val Ala Glu Thr Met Phe Tyr Pro Val Pro 930 935 940 Phe Thr Lys Leu Tyr Ser Asp Pro Leu Val Ala Ala Thr Leu His Pro 945 950 955 960 Leu Val Ala Asn Tyr Val Thr Arg Leu Pro Ala Gln Arg Val Pro Val 965 970 975 Ala Phe Asn Val Pro Pro Ala Leu Met Ala Glu Tyr Glu Glu Trp His 980 985 990 Lys Ser Pro Ile Leu Ala Tyr Ala Asn Thr Cys Pro Ile Thr Pro Thr 995 1000 1005 Ser Leu Ser Thr Leu Thr Ser Met His Met Lys Leu Ser Ala Pro 1010 1015 1020 Gly Phe Ile Cys His Ala Lys His Lys Ile His Pro Gly Phe Ala 1025 1030 1035 Met Thr Ala Val Arg Thr Asp Glu Val Leu Ala Glu Asn Leu Leu 1040 1045 1050 Phe Ser Ala Arg Ala Ser Thr Ser Met Phe Leu Gly Gln Pro Ser 1055 1060 1065 Val Met Arg Arg Glu Val Arg Ala Asp Ala Val Thr Phe Glu Val 1070 1075 1080 Asn His Glu Leu Ala Ser Leu Asp Met Ala Leu Gly Tyr Ser Ser 1085 1090 1095 Thr Ile Thr Pro Ala His Val Ala Ala Ile Thr Ser Asp Met Gly 1100 1105 1110 Val His Cys Gln Asp Leu Phe Leu Met Phe Pro Gly Asp Ser Tyr 1115 1120 1125 Gln Asp Arg Thr Leu Asn Asp Tyr Val Lys Gln Lys Ala Gly Cys 1130 1135 1140 Gln Arg Phe Gly Gly Pro Gly Gln Ile Arg Glu Pro Val Ala Tyr 1145 1150 1155 Val Ala Gly Val Pro His Ser Asp Asn Ile Pro Gly Leu Ser His 1160 1165 1170 Gly Gln Leu Ala Thr Cys Glu Ile Val Leu Thr Pro Val Thr Ala 1175 1180 1185 Asp Val Thr Tyr Phe Gln Thr Pro Asn Ser Pro Arg Gly Arg Ala 1190 1195 1200 Ser Cys Val Ile Ser Cys Asp Ala Tyr Asn Asn Glu Ser Ala Glu 1205 1210 1215 Arg Leu Leu Phe Asp His Ser Ile Pro Asp Ser Ala Tyr Glu Tyr 1220 1225 1230 Arg Thr Thr Val Asn Pro Trp Ala Ser Gln Gln Gly Ser Leu Gly 1235 1240 1245 Asp Val Leu Tyr Asn Ser Thr Ser Arg Gln Val Ala Val Pro Gly 1250 1255 1260 Met Tyr Ser Pro Cys Arg Gln Phe Phe His Lys Asp Ala Ile Leu 1265 1270 1275 Arg Asn Asn Arg Gly Leu Asn Thr Leu Val Thr Glu Tyr Ala Ala 1280 1285 1290 Arg Leu Thr Gly Thr Pro Ala Thr Ser Ala Thr Asp Leu Gln Tyr 1295 1300 1305 Val Val Val Asn Gly Thr Asp Val Phe Leu Glu Gln Pro Cys Gln 1310 1315 1320 Phe Leu Gln Glu Ala Phe Pro Thr Leu Ala Ala Ser His Arg Ala 1325 1330 1335 Leu Leu Asp Glu Tyr Met Ser Asn Lys Leu Thr His Ala Pro Val 1340 1345 1350 His Met Gly His Tyr Met Ile Glu Glu Val Ala Pro Met Lys Arg 1355 1360 1365 Leu Leu Lys Ile Gly Asn Lys Val Ala Tyr 1370 1375 47 107 PRT Japanese Macaque Herpesvirus 47 Met Ser Cys Cys Thr Arg Pro Arg Thr Arg Arg Phe Val Trp Arg Phe 1 5 10 15 Ile Arg Cys Leu Ile Phe Leu Phe Ile Ser Ser Gln Val Arg Lys Pro 20 25 30 Arg Ile Gly Leu Pro Thr Gly Leu Trp Trp Val Thr Phe Arg Asn His 35 40 45 Trp Arg Pro Thr Ser Phe Lys Thr Ala Glu Ala Cys Ser Leu Thr Glu 50 55 60 Arg Arg Pro Trp Leu Thr Cys Trp Thr Ser Gln Pro Trp Lys Leu Ser 65 70 75 80 Lys Ile Arg Arg Leu Thr Arg His Thr His Cys Phe Val Met Ser Leu 85 90 95 Asn Ala Ser Ser Thr Asp Arg Lys Thr Asn Phe 100 105 48 146 PRT Japanese Macaque Herpesvirus 48 Met Ile Arg Val Val Ser Gly Phe Val Asn Val Asn His Val Thr Asp 1 5 10 15 Glu Val Leu His Phe Ser Ser Asp Val Asn Val Arg Ile Pro Val Ile 20 25 30 Phe Arg Phe Val Pro Leu Val Ser Tyr Glu Tyr His Arg Val Pro Arg 35 40 45 Gly Leu Pro Lys Gln Val Gly Lys Asn Val Ile Val Ser Lys Gly Arg 50 55 60 Gln Lys Ile Gly Val Leu Lys Thr Val Asn Gln Leu Gly Arg Trp Pro 65 70 75 80 Ala Ser His His Leu Val Ala Ser Asn Phe Arg Glu Arg Leu Leu Gln 85 90 95 Asn Asn Glu Leu Ala Lys Asn Phe Ser Val Met Gly Val His Val Leu 100 105 110 Arg Asn Thr Thr Val Ala Gln Val Asn Ala Asp Lys Ser Gln His Arg 115 120 125 Glu Ala Val Asn Lys Arg Gln Phe Ser Gly Val Val Pro Val Gly Phe 130 135 140 Asn Gly 145 49 83 PRT Japanese Macaque Herpesvirus 49 Met Thr Gly Ile Arg Thr Leu Thr Ser Glu Glu Lys Trp Arg Thr Ser 1 5 10 15 Ser Val Thr Trp Leu Thr Phe Thr Lys Pro Glu Thr Thr Arg Ile Met 20 25 30 Thr Ala Ala Thr Ser Leu Thr Ser Val Pro Leu Thr Lys Thr Asn Ser 35 40 45 Thr Trp Arg Cys Trp Lys Ser Ser Phe Ile Thr Trp Ser Cys Gln Pro 50 55 60 Val Pro Thr Ala Thr Ser Ala Ala Trp Ala Ser Ile Leu Thr Thr Trp 65 70 75 80 Pro Trp Pro 50 305 PRT Japanese Macaque Herpesvirus 50 Met Ala Leu Asp Lys Ser Ile Val Val Ser Val Thr Ser Arg Leu Phe 1 5 10 15 Ala Asp Glu Ile Ala Asn Leu Gln Ser Lys Ile Gly Cys Ile Leu Pro 20 25 30 Leu Arg Asp Ala His Arg Leu Gln Asn Ile Gln Ala Leu Gly Leu Gly 35 40 45 Asn Leu Cys Ser Arg Asp Ser Ala Val Asp Phe Ile Gln Ala Tyr His 50 55 60 Tyr Leu Asp Lys Cys Thr Leu Ala Val Leu Glu Glu Val Gly Pro Asn 65 70 75 80 Ser Leu Arg Leu Thr Arg Ile Asp Pro Met Asp Asn Tyr Gln Ile Lys 85 90 95 Asn Ala Tyr Gln Pro Ala Phe His Trp Asp Asn Tyr Ser Glu Leu Val 100 105 110 Val Ile Pro Pro Val Phe Gly Arg Lys Asp Ala Thr Val Ser Leu Glu 115 120 125 Ser Asn Gly Phe Asp Val Val Phe Pro Ala Val Val Pro Glu Pro Leu 130 135 140 Ala Gln Thr Val Leu Gln Lys Leu Leu Leu Tyr Asn Ile Tyr Tyr Arg 145 150 155 160 Val Ala Glu Thr Thr Pro Thr Asp Val Asn Leu Ala Glu Val Thr Leu 165 170 175 Tyr Thr Thr Asn Ile Thr Tyr Met Gly Arg Asn Tyr Ala Leu Asp Met 180 185 190 Asp Pro Val Gly Ser Ser Ser Ala Met Arg Met Leu Asp Asp Leu Ser 195 200 205 Ile Tyr Leu Cys Val Leu Ser Ala Leu Ile Pro Arg Gly Cys Val Arg 210 215 220 Leu Leu Thr Ser Leu Val Arg His Asn Lys His Glu Leu Val Glu Ile 225 230 235 240 Phe Glu Gly Val Val Pro Pro Glu Val Gln Ala Leu Asp Leu Asn Asn 245 250 255 Val Ser Val Ala Asp Asp Ile Thr Arg Met Gly Ala Leu Met Thr Tyr 260 265 270 Leu Arg Ser Leu Ser Ser Ile Phe Asn Leu Gly Arg Arg Leu His Val 275 280 285 Tyr Ala Phe Ser Ser Asp Thr Asn Thr Ala Ser Cys Trp Cys Ala Tyr 290 295 300 Asn 305 51 274 PRT Japanese Macaque Herpesvirus 51 Met Ser Ile Pro Lys Ile Met Thr Val Ser Arg Asp Asn Glu Gly Thr 1 5 10 15 Val Cys Glu Val Ala Val Asp Asn Gly Arg His Arg Ala Met Ile Tyr 20 25 30 Tyr Pro Lys Ile Thr Asn Ser Ser Asn Glu Arg Ala Ala Gln Arg Ala 35 40 45 Asp Val Val Lys Glu Ala Phe Asp Thr Glu Thr Pro Val Asp Ile Val 50 55 60 Lys Gln Ile Val Asn Glu Gly Leu Ala Ile Ser Lys Arg Asn Cys Val 65 70 75 80 Arg Leu Ala Leu Tyr Leu Tyr Phe Tyr Leu Gln Tyr Val Cys Phe Ala 85 90 95 Ile Leu Ile Thr Trp Gln Leu Asn Pro His Ile Asp Pro Pro Gly Leu 100 105 110 Val Phe Ala Val Asn Pro Met Gly Pro Lys His Val Ser Lys Leu Pro 115 120 125 His Pro Ala Ile Val Ala Val Gly Cys Gly Thr Asp Ala Ile Cys Lys 130 135 140 Asn Cys Ser Val Pro Asp Ile Lys Thr Glu Leu Gly Val Val Tyr His 145 150 155 160 Asn Gly Ser Ser Asp Ser Gly Gln Ser Ala His Tyr Gly Leu Ala Leu 165 170 175 Leu Lys Ala Ala Trp Leu Val Met Gly Asn Val Cys Pro Glu Pro Val 180 185 190 Val Arg Gln Gly Ala Glu Leu Leu Gly Pro Trp Asn Arg Thr Ala Trp 195 200 205 Leu Asp Phe Lys Ser Ala Met Ala Ala Thr Thr Phe Cys Gly Ser Arg 210 215 220 Gly Val Leu Trp Ser Pro Ile His Glu Lys Asn Leu Cys Arg Pro Thr 225 230 235 240 Trp Asn Asp Val Ile Asn Thr Ser Ser Phe Phe Thr Asn Glu Ser Leu 245 250 255 Cys Pro Asn Val Pro Gly Val Ser Glu Ile Val Ile Val Leu Asn Gly 260 265 270 Asp Ala 52 91 PRT Japanese Macaque Herpesvirus 52 Met Thr Ala His Thr Asn Gly Val Leu Thr Thr Thr Gly Val Ser Thr 1 5 10 15 Ser Gln Pro Glu Ser Phe Gln Ile Ser Pro Phe Phe Arg Val Ile Thr 20 25 30 Lys Pro Pro Ile Met Gly Leu Phe Phe Cys Val Ala Met Cys Ile Ile 35 40 45 Ala Leu Val Trp Tyr Val Met Arg Arg Val Tyr Cys Lys Gly Arg Val 50 55 60 Val Ala Asp Ser Cys Arg Asp Pro Arg Arg Pro Ala Tyr Glu Met Leu 65 70 75 80 Asn Val Arg Leu Arg Pro His Gly Thr Asn Pro 85 90 53 348 PRT Japanese Macaque Herpesvirus 53 Met Leu Gln Lys Asp Ala Lys Leu Ile Phe Ile Ser Ser Ser Asn Ser 1 5 10 15 Ser Asp Lys Ser Thr Ser Phe Leu Leu Asn Leu Lys Asp Ala His Glu 20 25 30 Lys Met Leu Asn Val Val Ser Tyr Val Cys Pro Asp His Lys Asp Asp 35 40 45 Phe Asn Leu Gln Asp Thr Val Val Ala Cys Pro Cys Tyr Arg Leu His 50 55 60 Ile Pro Ala Tyr Ile Thr Ile Asp Glu Thr Val Arg Ser Thr Thr Asn 65 70 75 80 Leu Phe Leu Asp Gly Ala Phe Ser Thr Glu Leu Met Gly Asp Ala Ala 85 90 95 Thr Ser Ala Gln Ser Met His Lys Ile Val Ser Asp Ser Ser Leu Ser 100 105 110 Gln Leu Asp Leu Cys Arg Val Glu Ser Thr Ser Gln Asp Ile Gln Gly 115 120 125 Ala Met Lys Pro Phe Leu His Val Tyr Ile Asp Pro Ala Tyr Thr Asn 130 135 140 Asn Thr Asp Ala Ser Gly Thr Gly Ile Gly Ala Val Ile Ala Val Asn 145 150 155 160 His Lys Val Ile Lys Cys Ile Leu Leu Gly Val Glu His Phe Phe Leu 165 170 175 Arg Asp Leu Thr Gly Thr Ala Ala Tyr Gln Ile Ala Ser Cys Ala Ala 180 185 190 Ala Leu Ile Arg Ala Ile Val Thr Leu His Pro Gln Ile Leu His Val 195 200 205 Asn Val Ala Val Glu Gly Asn Ser Ser Gln Asp Ala Gly Val Ala Ile 210 215 220 Ala Thr Val Leu Asn Glu Ile Cys Ser Val Pro Leu Ser Phe Leu His 225 230 235 240 His Ala Asp Lys Asn Thr Leu Ile Arg Ser Pro Ile Tyr Met Leu Gly 245 250 255 Pro Glu Lys Ala Lys Ala Phe Glu Ser Phe Ile Tyr Ala Leu Asn Ser 260 265 270 Gly Thr Phe Ser Ala Ser Gln Thr Val Val Ser His Thr Ile Lys Leu 275 280 285 Ser Phe Asp Pro Val Ala Tyr Leu Ile Asp Gln Ile Lys Ala Ile Arg 290 295 300 Cys Ile Pro Leu Lys Asp Gly Gly His Thr Tyr Cys Ala Lys Gln Lys 305 310 315 320 Thr Met Ser Asp Asp Val Leu Val Ala Thr Val Met Ala His Tyr Met 325 330 335 Ala Thr Asn Asp Lys Phe Val Phe Lys Ser Leu Glu 340 345 54 217 PRT Japanese Macaque Herpesvirus 54 Met Ser Phe Leu Tyr His Asn Arg Cys Lys Glu Cys Gln Met Thr Arg 1 5 10 15 Val Asn Ser Pro Ile Cys Gln Phe His Asn Val Ser Ser Leu Tyr Gln 20 25 30 Cys Leu Asp Cys Lys Arg Tyr His Val Cys Asp Gly Gly Arg Asp Cys 35 40 45 Val Ile Val Tyr Thr Arg Glu Asn Leu Val Cys Asp Leu Thr Gly Asn 50 55 60 Cys Val Leu Asp Asn Val Gln Asp Val Cys Ser Tyr Gly Pro Pro Glu 65 70 75 80 Arg Arg Ala Pro Asp Ala Phe Ile Asp Pro Leu Val Ser His Gly Thr 85 90 95 Arg Glu Ser Leu Lys Ser Asp Ile Leu Arg Tyr Phe Glu Thr Val Gly 100 105 110 Val Lys Ser Glu Ala Tyr Ser Thr Val Val Lys Asn Gly Gln Leu Asn 115 120 125 Gly Ile Ile Gly Arg Leu Ile Asp Ala Thr Phe Asn Glu Cys Leu Pro 130 135 140 Val Met Ser Asp Gly Glu Gly Gly Arg Asp Leu Ala Ala Ser Ile Tyr 145 150 155 160 Ile His Ile Ile Ile Ser Ile Tyr Ser Thr Lys Thr Val Tyr Asp Asn 165 170 175 Leu Leu Phe Lys Cys Thr Arg Asn Lys Lys Tyr Asp His Ile Val Lys 180 185 190 Thr Ile Arg Ala Gln Trp Met Arg Met Val Ser Thr Gly Asp Pro Ser 195 200 205 Arg Val Asn Ala Thr Gly Cys Phe Thr 210 215 55 119 PRT Japanese Macaque Herpesvirus 55 Met Leu Ala Ala Arg Ser Leu Pro Pro Ser Pro Ser Leu Ile Thr Gly 1 5 10 15 Arg His Ser Leu Asn Val Ala Ser Ile Asn Leu Pro Met Met Pro Phe 20 25 30 Ser Cys Pro Phe Leu Thr Thr Val Glu Tyr Ala Ser Asp Phe Thr Pro 35 40 45 Thr Val Ser Lys Tyr Leu Asn Ile Ser Leu Leu Arg Leu Ser Leu Val 50 55 60 Pro Cys Asp Thr Arg Gly Ser Met Asn Ala Ser Gly Ala Arg Arg Ser 65 70 75 80 Gly Gly Pro Tyr Glu His Thr Ser Cys Thr Leu Ser Lys Thr Gln Phe 85 90 95 Pro Val Lys Ser His Thr Arg Phe Ser Arg Val Tyr Thr Met Thr Gln 100 105 110 Ser Arg Pro Pro Ser His Thr 115 56 461 PRT Japanese Macaque Herpesvirus 56 Met Asp Ala His Gly Leu Asn Arg Arg Ser Val Ala Gly Gln Cys Asp 1 5 10 15 Gly Leu Phe His Val Ile Leu Pro Arg Gly Phe Ile Leu Ala Asn Asn 20 25 30 Ile Thr Cys Gly Gly Arg Gln Arg Phe Phe Ala His Thr Arg Phe Ala 35 40 45 Ala Ser Glu Arg Thr Ser Lys Thr Leu Tyr Val Trp Gly Arg Val Phe 50 55 60 Gln Asn Thr Asp Pro Gly Ser Gly Asp Gly Pro Ser Gly Pro Trp Ser 65 70 75 80 Gly Leu Ala Ile Ser Leu Pro Leu Phe Thr Thr Asn Gly Lys Phe His 85 90 95 Pro Phe Asp Val Val Ile Leu Arg Ala Glu Thr Pro Gly Ser Gly Ser 100 105 110 Ser Trp Thr Val Lys Phe Leu Tyr Met Ser Leu Ile Ala Ala Tyr Arg 115 120 125 Asn Ala Met Arg Gly Leu Lys Asp Lys Val Ser Gln Ser Thr Asp Ala 130 135 140 Ala Val Asp Gly Glu Val His Pro Leu Thr Val Leu Lys Glu Ala Leu 145 150 155 160 Val Ser Pro Asp Thr Ala Thr Arg Pro Val Ser Ala Cys Asn Pro Leu 165 170 175 Gln Met Leu Thr Gly Leu Leu Gln Ser Arg Val Arg Asp Asp Tyr Val 180 185 190 Thr His His Arg Ala Leu Glu Arg Pro Gly Asn Val Arg Gly Gln Val 195 200 205 Ser Ala Pro Thr Arg Thr Glu Met Pro Asn Gly Ser Pro Ser Arg Val 210 215 220 Arg Leu Gly Phe Arg Pro Pro Lys Gln Ala Asn Tyr Pro Lys Thr Trp 225 230 235 240 Ala Gln Ala Arg His Val Phe Ser Ser Arg Thr Tyr Tyr Val Cys Val 245 250 255 Tyr Asp Asn Glu Glu Leu Asp Thr Lys Trp Gln Arg Gln Asp Pro Arg 260 265 270 Pro Leu Ser Leu Asp Trp Ser Asp Pro Val Ala Tyr Leu Leu Glu Gly 275 280 285 Asp Leu Phe Leu Gly Ala Lys Gln Asn Ala Phe Val Asp Ser Leu Glu 290 295 300 Lys Thr Cys Arg Cys Gln Asn Tyr Thr Ile Lys Gln Phe Phe Pro Val 305 310 315 320 Ser Ile Asn Arg Asp Asn Asp Thr Val Asp Leu Ile Lys Glu His Phe 325 330 335 Ile Glu Ala Cys Leu Val Ile Arg Asn Gln Ala Ser Glu Arg Ser Ala 340 345 350 Trp Val Lys Ala Ala Leu Phe Arg Asn Asp Ser Asn Thr Tyr Trp Lys 355 360 365 Asp Val Leu Gly Leu Trp Glu His Gly Pro His Lys Leu Gly Thr Ala 370 375 380 Ile Lys Arg Pro Thr Ser Glu Pro Cys Asn Ala Asp Ile Asp Trp Ser 385 390 395 400 Trp Leu Leu Cys Asp Ala Asp Ile Thr Arg Ser Ile Asn Gly Gln Ser 405 410 415 Thr Val Cys Leu Val Val Ser Pro Ala Leu Ile Ala Trp Leu Val Leu 420 425 430 Pro Gly Gly Phe Val Ile Lys Gly Arg Tyr Asp Leu Ser Ser Glu Asp 435 440 445 Leu Met Phe Val Ala Ser Arg Tyr Gly His Pro Ala Ala 450 455 460 57 336 PRT Japanese Macaque Herpesvirus 57 Met Ala Thr Gln Arg Arg Asp Ile Leu Lys Ser Phe Leu Asn Lys Glu 1 5 10 15 Cys Ile Trp Leu Arg His Pro Gly Thr Ser Ala Phe Val Arg Val Tyr 20 25 30 Thr Ala Thr Thr Ala His Ser Ala Val Phe Asp Pro Pro Val Thr Ser 35 40 45 Glu Asp Ala Met Ser His Asn Cys Leu Asn Val Met Ile Met Leu Met 50 55 60 Lys Pro Lys Glu Phe Gly Pro Cys Val Thr Val Tyr Ile Asn Gly Asp 65 70 75 80 Ile Leu Asp Phe Cys Ala Thr Glu Tyr Val Ala Ile Arg Glu Val Pro 85 90 95 Gly Arg Ala Asp Leu Cys Leu Ile Arg Phe Gly Thr Leu Ser Asn Ala 100 105 110 Pro Arg Ser Val Pro Ile Pro Gly Pro Leu Asn Pro His Pro Arg Glu 115 120 125 Asn Val Pro Gly Leu Thr Lys Gln Glu Ile Ile Tyr Thr Ser Gln Thr 130 135 140 Val Pro Arg Ala Gln Ile Gln Asp Ala Ile Lys Gly Lys Ala Phe Lys 145 150 155 160 Gln Ile Asn Pro Phe Val Trp Phe Asp Gly Gly Ala Phe Trp Gln Leu 165 170 175 Phe Leu Ser Val Asp Tyr Met Leu Leu Cys Pro Ala Leu Glu Ile Val 180 185 190 Pro Ser Leu Ala Arg Ile Val Gly Leu Leu Thr Gln Cys Asp Lys Ser 195 200 205 Thr Cys Lys Ile Cys Thr Leu Ala His Val His Val Asn Ala Tyr Arg 210 215 220 Gly Tyr Thr Pro Pro Asp Ser Gln Gly Thr Ser Pro Ser Cys Pro Cys 225 230 235 240 Leu Ile Ser Cys Gly Ala Arg His Ala Thr Asp Val Leu Val Thr Gly 245 250 255 His Val Asn Leu Leu Gly Leu Leu Phe Asp Pro Lys Val Leu Pro Lys 260 265 270 Val Ser Arg Leu Arg Leu Lys Arg Asn Pro His Pro Val Pro Ile Glu 275 280 285 Asp Ala Met Ser Gly Val Thr Ala Glu Gly Thr Glu Val Leu Pro Thr 290 295 300 Ser Gln Pro Trp Ala Leu Ile Arg Leu Pro Asp Leu Ala Ser Arg Val 305 310 315 320 Met Leu Tyr Gly Cys Gln Asn Leu Lys Thr Ile Cys Leu Arg Ser Tyr 325 330 335 58 122 PRT Japanese Macaque Herpesvirus 58 Met Ala Ser Cys Ile Cys Ala Leu Gly Thr Val Trp Glu Val Tyr Ile 1 5 10 15 Ile Ser Cys Phe Val Ser Pro Gly Thr Phe Ser Arg Gly Cys Gly Phe 20 25 30 Asn Gly Pro Gly Ile Gly Thr Leu Leu Gly Ala Leu Glu Arg Val Pro 35 40 45 Lys Arg Ile Lys His Arg Ser Ala Leu Pro Gly Thr Ser Leu Met Ala 50 55 60 Thr Tyr Ser Val Ala Gln Lys Ser Arg Ile Ser Pro Phe Met Tyr Thr 65 70 75 80 Val Thr His Gly Pro Asn Ser Phe Gly Phe Met Ser Ile Ile Met Thr 85 90 95 Phe Lys Gln Leu Cys Asp Ile Ala Ser Ser Leu Val Thr Gly Gly Ser 100 105 110 Lys Thr Ala Glu Cys Ala Val Val Ala Val 115 120 59 129 PRT Japanese Macaque Herpesvirus 59 Met Arg Ala His Gly Cys Glu Val Gly Ser Thr Ser Val Pro Ser Ala 1 5 10 15 Val Thr Pro Asp Met Ala Ser Ser Ile Gly Thr Gly Trp Gly Phe Leu 20 25 30 Phe Lys Arg Ser Leu Asp Thr Leu Gly Ser Thr Phe Gly Ser Lys Ser 35 40 45 Arg Pro Lys Arg Phe Thr Cys Pro Val Thr Arg Thr Ser Val Ala Cys 50 55 60 Leu Ala Pro His Glu Ile Arg Gln Gly His Glu Gly Glu Val Pro Cys 65 70 75 80 Glu Ser Gly Gly Val Tyr Pro Arg Tyr Ala Leu Thr Cys Thr Trp Ala 85 90 95 Ser Val His Ile Leu His Val Leu Leu Ser His Cys Val Arg Arg Pro 100 105 110 Thr Ile Leu Ala Arg Asp Gly Thr Ile Ser Arg Ala Gly Gln Ser Ser 115 120 125 Ile 60 327 PRT Japanese Macaque Herpesvirus 60 Met Leu Leu Thr Ser Tyr Arg Glu Arg Leu Gln Asn Asn Leu Arg Ala 1 5 10 15 Val Thr Asp Gly Gly Cys Glu Asn Trp Phe Arg Gln Pro Pro Val Ile 20 25 30 Ile Ser Gly Asn Asp Lys Thr Glu Arg Met Ala His Pro Cys Leu Gly 35 40 45 Val Ile His Ala Val Asn Ala Tyr Ser Ser Val Leu Asp Asp Tyr Leu 50 55 60 Gln Thr Tyr Arg Arg Leu Gln Glu Pro Met Pro Pro Pro Thr Leu Gly 65 70 75 80 Lys Pro Arg Ile Ser Ser His Ala Thr Leu Pro Arg Leu Thr Glu Glu 85 90 95 Leu Thr Asn Tyr Leu Arg Gln Thr Cys Cys Arg Val Arg Met Ala Asp 100 105 110 Ala Lys Asp Gln His Met Glu Tyr Gln Ser Ala Gln Arg Thr His Glu 115 120 125 Ala Phe Leu Glu Cys Pro Val Tyr Ala Glu Leu Arg Gln Phe Leu Ala 130 135 140 Asn Leu Ser Ser Phe Leu Asn Gly Ser Tyr Val Pro Gly Val Cys Cys 145 150 155 160 Leu Glu Pro Phe Gln Gln Gln Leu Ile Met His Thr Phe Tyr Phe Ile 165 170 175 Ala Ser Ile Lys Ala Pro Glu Lys Thr His Gln Leu Phe Ala Thr Phe 180 185 190 Lys Gln His Phe Gly Leu Phe Glu Thr Thr Asp Asp Val Leu Gln Thr 195 200 205 Phe Lys Gln Lys Ala Ser Val Phe Val Ile Pro Arg Arg His Gly Lys 210 215 220 Thr Trp Ile Val Val Ala Ile Ile Ser Val Leu Leu Ser Ser Val Glu 225 230 235 240 Asn Val His Val Gly Tyr Val Ala His Gln Lys His Val Ala Asn Ala 245 250 255 Val Phe Ser Glu Val Ile Ala Thr Leu Ser Arg Trp Phe Pro Ala Lys 260 265 270 Asn Leu Asn Ile Lys Lys Glu Asn Gly Thr Ile Val Tyr Ala Ser Pro 275 280 285 Gly Arg Arg Pro Ser Ser Leu Met Cys Ala Thr Cys Phe Asn Lys Asn 290 295 300 Val Ser Arg Leu Phe Leu Asn Ser Gly Ser Arg Ile Ala Leu His Asp 305 310 315 320 Trp Leu Asn Pro Ala Gly Glu 325 61 88 PRT Japanese Macaque Herpesvirus 61 Met Leu Ser Gly Pro Asn Gly Arg Arg Gln Gly Pro Ala His Gly Ile 1 5 10 15 Pro Ile Gly Pro Thr Asp Pro Arg Ser Phe Pro Arg Val Ser Cys Leu 20 25 30 Cys Arg Thr Ala Ala Ile Phe Ser Gln Pro Val Val Ile Phe Lys Trp 35 40 45 Glu Leu Arg Ala Arg Gly Leu Leu Pro Arg Ala Leu Ser Ala Thr Val 50 55 60 Asn His Ala His Val Leu Phe Tyr Arg Val Tyr Gln Ser Thr Arg Lys 65 70 75 80 Asp Thr Pro Val Ile Cys His Val 85 62 328 PRT Japanese Macaque Herpesvirus 62 Met Phe Pro Ser Ser Phe Leu Asn Asn Glu Asn Pro Glu Thr Gly Arg 1 5 10 15 Arg Phe Val Lys Gly Val Gln Leu Ala Leu Asp Leu Cys Asp Asn Thr 20 25 30 Pro Gly Gln Phe Lys Leu Val Glu Thr Pro Leu Asn Ser Phe Leu Leu 35 40 45 Val Ser Asn Val Leu Pro Glu Ser Arg Pro Val Arg Asp Cys Pro Gln 50 55 60 Ala Glu Gly Phe Asp Phe Glu His Ile His Leu Pro Lys Leu Thr Arg 65 70 75 80 Met Gln Arg Val Leu Gly Arg Tyr Cys Asp His Val Asn Asn Asp Asp 85 90 95 Asp Met Cys Val Asn Val Lys Ala Arg Ser Ser Asn Ala Gln Gly Ala 100 105 110 Leu Phe Tyr Leu Pro Tyr Gly Gln Asp Glu Trp Asn Trp Ala Leu Thr 115 120 125 Leu Arg Lys Asp Lys Leu Val Lys Met Ala Val Glu Gly Leu Ser Asp 130 135 140 Pro Thr Thr Trp Lys Gly Leu Glu Pro Val Asp Pro Leu Pro Leu Ile 145 150 155 160 Trp Leu Leu Phe Tyr Gly Pro Arg Ser Phe Cys Arg Glu Pro Glu Cys 165 170 175 Leu Tyr Glu Arg Asn Phe Gly Met Lys Gly Pro Ile Leu Leu Pro Pro 180 185 190 His Met Tyr Ala Pro Arg Lys Asp Val Met Thr Phe Val His His Val 195 200 205 Ile Lys Tyr Val Lys Phe Leu Tyr Val Asn Ala Gly Gly Gly Leu Glu 210 215 220 Thr Glu Leu Ser Pro Pro Phe Glu Ala Ser Arg Leu Arg Ser Ala Ile 225 230 235 240 Ala Arg Leu Gly Asp Val Glu Ala Asp Asp Ala Tyr Leu Ser Ala Lys 245 250 255 Cys Met Leu Cys His Leu Tyr Lys Gln Asn Asp Thr Ile Ser Ile His 260 265 270 Glu Thr His Val Gly Gly Val Ile Ala Leu Gly Gly Asp Gly Ala Arg 275 280 285 Tyr Ile Thr Ser Ser Val Arg Thr Gln Arg Cys Thr Ser Arg Gly Asp 290 295 300 Phe Val Leu Ile Pro Leu Tyr Asn Ile Glu Gly Leu Val Ser Met Ile 305 310 315 320 Arg Glu His Gly Leu Ser Asn Ser 325 63 148 PRT Japanese Macaque Herpesvirus 63 Met Trp Ser Phe Gly Asp Ser Ser Ser Thr Gly Thr Asp Ser Ser Leu 1 5 10 15 Ser Val Pro Arg Ile Ser Ser Ser Pro Tyr Ser Ser Ser Leu Arg Ser 20 25 30 Arg Thr Ala Ser Val Thr Ala Ser Asn Ser Ser Ile Phe Phe Leu Leu 35 40 45 Asn Pro Phe Ser Asn Pro Asn Ser Leu Cys Phe Ser Arg Ser Asp Val 50 55 60 Ser Ser Val Pro Thr Thr Val Ala Arg Leu Ser Phe Phe Phe Arg Leu 65 70 75 80 Ser Tyr Asp Arg Ser Asp Ser Leu Val Pro Leu Tyr Cys Ala Leu Asn 85 90 95 Thr Ala Leu Ser Ala Pro Asn Leu Ser Lys Thr Glu Met Asp Ser Phe 100 105 110 Leu Leu Ile Ser Asp Ser Ser Ser Asp Leu Ile Asn Asn Phe Leu Ala 115 120 125 Val Ala Glu Ala Met Phe Pro Tyr His Ala Tyr Glu Pro Phe Asn Val 130 135 140 Val Gln Arg Asp 145 64 149 PRT Japanese Macaque Herpesvirus 64 Met Ala Ser Ala Thr Ala Lys Lys Leu Leu Ile Lys Ser Glu Leu Glu 1 5 10 15 Ser Glu Ile Asn Lys Lys Leu Ser Ile Ser Val Phe Asp Arg Phe Gly 20 25 30 Ala Asp Ser Ala Val Phe Asn Ala Gln Tyr Lys Gly Thr Arg Glu Ser 35 40 45 Leu Arg Ser Tyr Asp Ser Leu Lys Lys Lys Asp Asn Leu Ala Thr Val 50 55 60 Val Gly Thr Leu Glu Thr Ser Leu Arg Glu Lys Gln Ser Glu Leu Gly 65 70 75 80 Leu Leu Lys Gly Phe Asn Arg Lys Lys Ile Glu Glu Phe Asp Ala Val 85 90 95 Thr Asp Ala Val Arg Asp Leu Lys Asp Glu Leu Tyr Gly Glu Leu Glu 100 105 110 Ile Leu Gly Thr Leu Asn Asp Glu Ser Val Pro Val Glu Glu Glu Ser 115 120 125 Pro Lys Asp His Ile Ile Arg Trp Lys Leu Glu Arg Leu Pro Arg Val 130 135 140 Cys Pro Lys Ser Pro 145 65 435 PRT Japanese Macaque Herpesvirus 65 Met Asn Leu Phe Pro Trp Lys Lys Ser Pro Gln Arg Thr Thr Leu Leu 1 5 10 15 Asp Gly Asn Trp Ser Val Cys Gln Glu Cys Ala Pro Lys Ala Leu Asp 20 25 30 Pro Ile Pro Lys Val Gln Thr Asp Leu Asp Arg Thr Ala Leu Ser His 35 40 45 Ile Thr Val Ile Arg Thr Arg Lys Thr Leu Ala Gln Leu Lys Ile Pro 50 55 60 Asn Thr Trp Ser Gln Cys Ser His Gln Ala Thr Asp Trp Thr Ala Val 65 70 75 80 Leu Gly Arg Gly Ser Tyr Gly Val Val Arg Ser Met Ser Leu Gly Arg 85 90 95 Cys Val Lys His Phe Gly Ser Arg Arg Glu Phe Phe Tyr Glu Cys Ile 100 105 110 Phe Asn Asp Ile Val Arg Ala Arg Arg Glu Lys His Pro Leu Asn Arg 115 120 125 Gly Gly Asp Arg Ile Leu Cys Phe Leu Glu Pro Cys Val Pro Cys Arg 130 135 140 Ala Leu Ile Phe Pro Gln Leu Thr Gly Asn Leu Leu Asn Ala Asp Phe 145 150 155 160 Lys His Val Asn Pro Glu Arg Leu Ala Val Glu Phe Ser Glu Leu Arg 165 170 175 Glu Gly Val Ser Phe Leu Asn Asn Ile Cys Gly Ile Val His Cys Asp 180 185 190 Ile Ser Pro Glu Asn Ile Leu Ile Lys Gly Glu Leu Thr Thr Ala Tyr 195 200 205 Trp Arg Leu Met Ile Gly Asp Leu Gly Ser Ala Ser Leu His Thr Gly 210 215 220 Thr Pro Trp Thr Gly Val Met Val Thr Ser Lys Leu Gly Phe Val Gln 225 230 235 240 His Thr Tyr His Phe Lys Ala Pro Ala Arg Phe Ile Cys Lys His Met 245 250 255 Tyr Arg Pro Ser Cys Leu Leu Tyr Arg Cys Leu Leu Ser Cys Ala Gly 260 265 270 Gly Pro Gln Ala Arg Met Leu Asp Gln Pro Phe Gln Ile Thr Pro Gln 275 280 285 Leu Gly Leu Thr Ile Asp Met Ser Ser Leu Gly Tyr Ser Leu Leu Ala 290 295 300 Cys Leu Glu Lys Tyr Leu Gln Pro Ala Asp Pro Phe Pro Gln Gln Gly 305 310 315 320 Ala Leu Ala Asp Ala Ser Ser Glu Ser Ala His Pro Leu Phe Tyr Leu 325 330 335 Arg Cys Met Val Pro Arg Val Val Ile Ala Glu Ile Phe Ser Val Ala 340 345 350 Trp Asp Val Pro Leu Asp Leu Gly Ile Asp Ser Ser Gly His Ala Pro 355 360 365 Ala Ile Pro Leu Arg Glu Ala Tyr Arg Arg Phe Phe Ala Asn Gln Cys 370 375 380 Ser Leu Tyr Arg Ala Gln Tyr Lys Glu Asp Ala Leu Glu Asn Ala Ser 385 390 395 400 Ser Arg Leu Cys Asn Ser Lys Leu Lys Leu Val Leu Gln Lys Leu Leu 405 410 415 Val Arg Asp Tyr Phe Ser His Cys Gly Asn Cys Gly Asp His Gly Phe 420 425 430 Phe Leu Arg 435 66 480 PRT Japanese Macaque Herpesvirus 66 Met Asp Phe Phe Ser Asp Glu Pro Met Val Gln Glu Met Ala Leu Leu 1 5 10 15 Asp Ile Asp Glu Gln Gln Arg His Leu Ser Lys Met Ser Leu Ala Asn 20 25 30 Phe Leu Lys His Glu Arg Val Arg Ala Phe Phe Asn Asp Asn Lys Lys 35 40 45 Lys Ile Ser Met Pro Ala Ile Arg Phe Val Tyr Asn Phe Tyr Leu Phe 50 55 60 Ala Lys Val Gly Asp Phe Ile Gly Asn Thr Glu Val Tyr Asp Phe Tyr 65 70 75 80 Val Ser Cys Val Phe Arg Gly Arg Arg Leu Thr Leu Leu Ser Asp Val 85 90 95 Tyr Asp Ala Cys Leu Asn Met His Pro His Asp Arg His His Val Cys 100 105 110 Ala Leu Ile Glu Gln Val Thr Arg Gly Gln Asn Ile Asn Pro Leu Trp 115 120 125 Asp Ala Leu Arg Asp Gly Ile Ile Ser Ser Ser Lys Phe His Trp Ala 130 135 140 Ile Lys Gln Gln Asn Ser Ser Lys Lys Ile Phe Asn Pro Trp Pro Ile 145 150 155 160 Val Asn Asn His Phe Ile Ala Gly Pro Leu Ala Phe Gly Leu Arg Cys 165 170 175 Glu Asp Val Val Lys Lys Ile Leu Ala Thr Leu Leu His Pro Gly Glu 180 185 190 Ala His Cys Glu Asn Tyr Gly Phe Met Gln Ser Pro His Asn Gly Val 195 200 205 Phe Gly Val Ser Leu Asp Phe Gly Ile Asn Val Lys Ser Asn Pro Lys 210 215 220 Asp Gly Leu Glu Phe His Pro Asp Cys Lys Ile Tyr Glu Ile Lys Cys 225 230 235 240 Arg Phe Lys Tyr Thr Phe Ser Lys Met Glu Cys Asp Pro Ile Tyr Ala 245 250 255 Ala Tyr Ala Lys Leu Tyr Gln Lys Pro Ser Met Gln Thr Leu Lys Gly 260 265 270 Phe Leu Tyr Ser Ile Ser Lys Pro Ala Ile Glu Phe Val Gly Glu Asp 275 280 285 Lys Leu Pro Ser Glu Ala Asp Tyr Leu Val Ala Tyr Asp Lys Glu Trp 290 295 300 Glu Val Cys Pro Arg Lys Lys Arg Arg Leu Thr Ala Val His His Leu 305 310 315 320 Val Lys Lys Cys Met Ile His Asn Ser Thr Ala Pro Ser Asp Val Tyr 325 330 335 Ile Leu Ser Asp Pro Gln Glu Thr Gly Gly Gln Ile Asn Ile Lys Ala 340 345 350 His Leu Ser Ala Asn Leu Phe Ile Asn Val Arg His Pro Tyr Tyr Tyr 355 360 365 Gln Val Leu Leu Gln Ser Leu Val Val Gln Glu Tyr Ile Ser Leu Ser 370 375 380 Lys Gly Thr Lys Asn Leu Gly Thr Gln Lys Asn Phe Ile Ala Thr Gly 385 390 395 400 Phe Phe Arg Lys Arg Gln Phe Gln Asp Pro Ser Asn Cys Thr Ile Gly 405 410 415 Glu Phe Ala Pro Leu Asp Pro His Val Glu Ile Pro Thr Leu Leu Ile 420 425 430 Val Thr Pro Val Tyr Phe Pro Ser Val Ala Lys His Gln Leu Val Lys 435 440 445 Gln Ala Thr Glu Phe Trp Ala Ala Ser Ala Ser Glu Ala Phe Pro Glu 450 455 460 Leu Pro Trp Asp Leu Ser Ser Leu Cys Ala Asn Ala Pro Pro Thr Pro 465 470 475 480 67 378 PRT Japanese Macaque Herpesvirus 67 Met Lys Ile Ser Arg Ser Asp Ser Phe Ile Leu Ser Ser Trp Val Lys 1 5 10 15 Leu Leu Val Ile Leu Gly Leu Met Phe Ile Met Ser Ala Val Val Pro 20 25 30 Leu Thr Ala Thr Phe Pro Gly Leu Gly Phe Pro Cys Tyr Phe Asn Thr 35 40 45 Leu Val Asn Tyr Ser Ala Leu Asn Leu Thr Val Arg Ser Ser Ala Lys 50 55 60 His Leu Thr Pro Thr Leu Phe Leu Glu Ala Pro Glu Met Phe Val Tyr 65 70 75 80 Ile Ser Trp Ala Phe Leu Val Asp Gly Tyr Leu Leu Cys Tyr Tyr Ala 85 90 95 Trp Ala Ile Leu Ala Ile Phe Lys Ala Lys Arg Val His Ala Thr Thr 100 105 110 Met Thr Ser Leu Gln Thr Trp Ile Val Leu Ile Gly Ser His Ser Val 115 120 125 Val Phe Met Ser Ile Leu Arg Leu Trp Thr Ile Gln Leu Phe Ile His 130 135 140 Val Leu Ser Tyr Lys His Ile Leu Leu Ala Ser Phe Val Tyr Cys Ile 145 150 155 160 His Phe Cys Leu Ser Phe Thr His Val Gln Ala Met Ile Ser Cys Asn 165 170 175 Ser Ala Thr Trp Ser Leu Arg Val Leu Glu Gln Gln Ile Pro Glu Asn 180 185 190 Ser Leu Leu Asp Thr Leu Leu Arg Tyr Gly Lys Pro Ile Gly Ala Asn 195 200 205 Leu Tyr Leu Ser Leu Ile Ala Met Glu Met Leu Val Phe Ser Leu Gly 210 215 220 Thr Met Met Ala Ile Gly Asn Ser Phe Tyr Met Leu Val Ser Asp Ile 225 230 235 240 Val Phe Gly Ser Ile Asn Leu Phe Phe Val Leu Thr Val Ala Trp Tyr 245 250 255 Ile Asn Thr Glu Leu Phe Leu Val Lys Tyr Leu Lys His Gln Ile Gly 260 265 270 Phe Tyr Val Gly Val Phe Val Ser Tyr Leu Ile Leu Leu Leu Pro Val 275 280 285 Val Arg Tyr Asp Lys Val Phe Ile Ser Ala Ser Leu His Lys Val Ile 290 295 300 Ala Val Asn Ile Ser Met Ile Pro Ile Thr Cys Ile Leu Ala Ile Ile 305 310 315 320 Leu Arg Ile Ile Arg Asn Asp Trp Lys Trp Cys Ala Lys Ala Pro Glu 325 330 335 Tyr Ala Pro Leu Pro Gln Gly Ser Lys Glu Lys Thr Thr Lys Val Lys 340 345 350 Tyr Ser Pro Glu Leu Asn Ala Leu Tyr Glu Thr Glu Glu Asp Val Ser 355 360 365 Asp Asp Glu Asp Ala Tyr Pro Lys Tyr Ile 370 375 68 104 PRT Japanese Macaque Herpesvirus 68 Met Tyr Thr Val Tyr Lys Arg Gly Gln Lys Tyr Met Phe Val Arg Gln 1 5 10 15 His Val Asn Lys Gln Leu Asn Gly Pro Gln Pro Gln Asn Arg His Lys 20 25 30 Asn Tyr Ala Val Arg Thr Tyr Glu His Asp Pro Gly Leu Glu Ala Gly 35 40 45 His Cys Arg Arg Val His Ala Leu Gly Leu Glu Tyr Gly Gln Asp Gly 50 55 60 Pro Arg Val Val Thr Gln Gln Ile Ser Val His Gln Lys Arg Pro Arg 65 70 75 80 Asp Val Asn Lys His Phe Trp Cys Phe Gln Lys Gln Arg Arg Arg Gln 85 90 95 Val Phe Ser Arg Thr Ser Asp Arg 100 69 667 PRT Japanese Macaque Herpesvirus 69 Met Asn Ala Arg Glu Val Ala Leu Thr Gly His Val Leu His Ile Ser 1 5 10 15 Leu His Ser Thr His Glu Arg Glu Lys Leu Ile Ile Trp Gln Val His 20 25 30 Leu Leu Val Cys Gln Gln Cys Gly Ile Gln Gly Asp Ala Ala Tyr Leu 35 40 45 Phe Val Thr Glu Thr Leu Ser Asn Thr Asp Trp Gly Asn Ile Pro Ala 50 55 60 Ile Asn Arg His Ala Pro Ser Met Asn Glu His Gly Arg Asn Tyr Met 65 70 75 80 Gln Trp Glu Leu Arg Thr Arg Leu Arg Asn Pro Ile Ile Gln Ser Leu 85 90 95 Ser Arg Gln Pro Gly Ala Val Asn Val Arg Val Ser Glu Pro Asn Met 100 105 110 Val Ile Val Ser Cys Glu Arg Ala Leu His His Ser Cys Ser Val Arg 115 120 125 Val Thr Gly Ala Tyr Leu His Cys Asn Thr Thr Met Asp Phe Arg Leu 130 135 140 Asp Ser Asn Val Ser Pro Thr Arg Glu Phe Trp Phe Ser Glu Met Phe 145 150 155 160 Ser Lys Cys Leu Val Ser Asn Ile Glu Val Tyr Leu Lys Thr Thr Gly 165 170 175 Gly Leu Tyr Tyr Arg Ala Ser Ser Ala Thr Gln Cys Arg Lys Arg Ala 180 185 190 Lys Asp Gly Ala Leu Gly Ile Leu Asp Ile Phe Asn Cys Glu Ser Arg 195 200 205 Glu Ile Gln Val Ala Gly Gln Lys Tyr Asn Leu Ser Ile Ala Thr Ala 210 215 220 Thr Phe His Val Leu Trp Val Asp Glu Ala Cys Met Trp Asn Gly Ala 225 230 235 240 Leu Ala Glu Phe Phe Arg Ala Leu His Asn Lys Leu Phe Gly Asp Arg 245 250 255 Glu Gly Val Ala Pro Thr Leu Thr Tyr Val Cys Pro Gly Ala Thr Pro 260 265 270 Glu Gly Thr Pro Phe Pro Pro Tyr Phe Ser Ala Phe Pro His Leu Leu 275 280 285 Leu Val Phe Gly Arg Pro Arg Arg Leu Asp Val Thr Ala Val Gln Glu 290 295 300 Leu Pro Lys Ala Gln Ile Ala Val His Trp Pro Pro Phe Lys Asn Ser 305 310 315 320 Ile Leu Gly Asp Gln Leu Leu Ile Pro Gly Ile Ser Pro Lys Lys Pro 325 330 335 Gly Thr Val Pro Val Arg Trp Pro Leu Trp Val Gln Asp Val Asn Leu 340 345 350 Ser Leu Cys Glu Thr Thr Glu Ser Val Ala Arg Ile Val Asp Pro His 355 360 365 Ser Ile Val Ile Ile Lys Ile Ser Thr Leu Leu Cys Gln His Leu Lys 370 375 380 Cys His Arg Ala Phe Val Lys Asn Glu Leu Glu Tyr Ile Ala Thr Ile 385 390 395 400 Cys Ser Ser Asp Leu Arg Leu Phe Ile Gln Glu Glu Tyr Asn Arg Leu 405 410 415 Leu Ala Thr Ile Phe Thr Trp Ala Ala Ala Ser Gly Tyr Thr Trp Ala 420 425 430 Ala Ile Asp Lys Thr Thr Val Phe Ile Lys Ala Pro Gln Leu Ser Ala 435 440 445 Ala Val Ser Gly Ser Cys Pro Ser Leu Asn Ser Cys Arg Arg Lys Gln 450 455 460 Tyr Tyr Lys Gly Leu Lys Ile Thr Val His Phe Leu Ser Gln Glu Gln 465 470 475 480 Gln Lys Val Val Thr Arg Leu Glu Ala Gln Leu Gly Leu Pro Val Gln 485 490 495 Glu Thr Ser Arg Pro Pro Asp Trp Leu Lys Tyr Glu Val Cys Ser Ala 500 505 510 Ser Val Phe Leu Lys Ile Pro Ala Gly Val Leu Tyr Ala Gly Leu Ala 515 520 525 Lys Asp Pro Val Ser Glu Ala Lys Arg Asp Ser Trp Leu Asp Cys Leu 530 535 540 Val Glu Gly Ala Thr Leu Ser Leu Asn Asn Ser Val Pro Pro Ile Gly 545 550 555 560 Ala Leu Ala Gly Ile Leu Pro Thr Leu Phe Ala Lys Arg Arg Cys Val 565 570 575 Asn Phe Trp Leu Leu Pro Arg Glu Trp Val Lys Ser Ala Pro Ile Cys 580 585 590 Pro Pro Leu Pro Ile Asp Cys Val Thr Pro Gln Gln Phe Val Val Thr 595 600 605 Lys Arg Gly Pro Ile Cys Trp Tyr Lys Glu Trp Pro Leu Pro Val Asp 610 615 620 Val Asp Phe Met Tyr Tyr Leu Gln Glu Ala Leu Cys Val Phe Ser Val 625 630 635 640 Val Ser Asn Gly Glu Gly Thr Glu Ser His Ala Asp Asp Ile Arg Gln 645 650 655 Leu Glu Lys Phe Glu Lys Val Leu Cys Leu Phe 660 665 70 116 PRT Japanese Macaque Herpesvirus 70 Met Asn Thr Val Val Leu Ser Met Ala Ala Gln Val Tyr Pro Leu Ala 1 5 10 15 Ala Ala His Val Lys Ile Val Ala Ser Asn Arg Leu Tyr Ser Ser Trp 20 25 30 Met Lys Arg Arg Arg Ser Leu Glu Gln Met Val Ala Met Tyr Ser Asn 35 40 45 Ser Phe Leu Thr Asn Ala Arg Trp His Phe Arg Cys Trp His Asn Ser 50 55 60 Val Glu Ile Phe Met Ile Thr Ile Glu Cys Gly Ser Thr Met Arg Ala 65 70 75 80 Thr Leu Ser Val Val Ser Gln Arg Leu Lys Leu Thr Ser Cys Thr Gln 85 90 95 Ser Gly Gln Arg Thr Gly Thr Val Pro Gly Phe Leu Gly Glu Met Pro 100 105 110 Gly Met Arg Ser 115 71 271 PRT Japanese Macaque Herpesvirus 71 Met Asp Gln Ile Leu Lys Arg Leu Met Gly Glu Gln His Arg Ser Glu 1 5 10 15 Ala Ile Met Pro Glu Thr Glu Cys Ala Ser Arg Gly Pro Tyr Asn Tyr 20 25 30 Pro Val Leu Pro Arg Leu Met Leu Glu Val His Lys Lys Asn Ser Ile 35 40 45 Cys Met Ala Ser Asn Thr Pro Lys Leu Cys Val Arg Gly Arg Leu Asn 50 55 60 Val Pro Asp Leu Gly Val His Val Arg Thr Arg Leu Gln Ser Ala Thr 65 70 75 80 Phe Thr Gly Phe Val Phe Ala Cys Val Val Glu His Glu Asp Met Val 85 90 95 Asn Thr Leu Asp Ile Tyr Pro His Val Phe Ser Asp Arg Val Gln Leu 100 105 110 Phe Lys Pro Ala Ser Ala Ser Val Thr Glu Leu Cys Cys Ile Leu Ser 115 120 125 Met Leu Glu Asn Tyr Asp Lys Pro Pro Leu Ser Phe Ile Leu Ser Ala 130 135 140 Leu Asp Arg Ala Arg Tyr Leu His Glu Arg Tyr Thr Cys Asn Asp Ser 145 150 155 160 Ala Phe Ile Leu Tyr Gly Ile Glu Val Ile Ala Ser Thr Leu Ala Ala 165 170 175 Tyr His Glu Leu Asn Pro Pro Gln Gly Val Leu Arg Val Pro Pro Leu 180 185 190 Val Arg Phe Lys Leu His Lys Leu Leu Asp Glu Asn Ala Asp Asp Met 195 200 205 Lys Gly Leu Leu Lys Pro Ile Tyr Leu Glu Ser Phe Arg Leu Thr Glu 210 215 220 Asn Val Glu Glu Asp Ser His Gly Glu Thr Phe Asn Ile Phe Tyr Cys 225 230 235 240 Gly Thr Ile Phe Thr Arg His Leu His Asn Ala Ser Val Leu Lys Tyr 245 250 255 Phe Gln Ile Thr Ser Leu His Ser Leu Pro Arg Gln Thr Leu Phe 260 265 270 72 82 PRT Japanese Macaque Herpesvirus 72 Met Gly Phe Ser Lys Pro Phe Met Ser Ser Ala Phe Ser Ser Asn Ser 1 5 10 15 Leu Trp Ser Leu Asn Arg Thr Arg Gly Gly Thr Arg Lys Thr Pro Trp 20 25 30 Gly Gly Phe Asn Ser Trp Tyr Ala Ala Lys Val Asp Ala Ile Thr Ser 35 40 45 Ile Pro Tyr Asn Ile Asn Ala Glu Ser Leu His Val Tyr Leu Ser Cys 50 55 60 Arg Tyr Leu Ala Arg Ser Ser Ala Asp Arg Ile Asn Asp Arg Gly Gly 65 70 75 80 Leu Ser 73 581 PRT Japanese Macaque Herpesvirus 73 Met Phe Lys Met Asn Pro Gly Leu Gly Ser Thr Cys Leu Val His Pro 1 5 10 15 Thr Glu Leu Ser Ile Ser Leu Phe Glu Ile Leu Gln Gly Lys Tyr Ala 20 25 30 Tyr Val Arg Gly Gln Thr Leu His Ser Ser Leu Arg Asn Pro Gly Ile 35 40 45 Phe Gly Arg Gln Leu Phe Ile His Leu Tyr Lys Thr Ala Leu Gly Ser 50 55 60 Cys Thr Tyr Asp Asn Val Leu Lys Asp Trp Thr Asn Phe Glu Thr Thr 65 70 75 80 Leu Lys Thr Arg Trp Arg Gly Val Glu His Leu Thr Pro Glu Phe Lys 85 90 95 Arg Ser Thr Phe Glu Ser Trp Ala Arg Thr Val Arg Leu Thr Val Asp 100 105 110 Gln Leu Leu Leu Asn Thr Ile Asn Gln Val Leu His Thr Arg Thr Val 115 120 125 Leu Ser Tyr Glu Arg Tyr Val Asp Trp Val Val Ala Leu Gly Leu Val 130 135 140 Pro Ile Val Arg Arg Ala Pro Asp Gly Glu Thr Ile Ala Arg Ile Gln 145 150 155 160 Ala His Cys Gln Gln Met Arg Lys Thr His Ala Ser Gly Asp Val Thr 165 170 175 Ile Ser Arg Ile Val Asp Lys Leu Ala Gln Glu Ile Thr Ala Ile Met 180 185 190 Thr Asp Val Thr Ser Ile Tyr Ile Pro Asp Tyr Ala Glu Val Ser Val 195 200 205 Glu Phe Asn Gly Asp Lys Ala Ala Tyr Leu Gly Thr Tyr Arg Gln Lys 210 215 220 Asp Ile Thr Val Glu Val Val Ser Arg Pro Ile Ile Tyr Asn Gly Arg 225 230 235 240 Val Ser Phe Asp Ser Pro Leu Tyr Arg Leu Phe Thr Ala Ile Met Thr 245 250 255 Cys His Arg Thr Ala Glu His Ala Lys Leu Cys Gln Leu Leu Asn Thr 260 265 270 Ala Pro Leu Lys Ala Leu Val Gly Ser Thr Cys Asn Asp Met Tyr Lys 275 280 285 Asp Ile Leu Ala Arg Leu Glu Gln Ser Ser Gln Lys Thr Asp Pro Lys 290 295 300 Arg Glu Leu Leu Asn Leu Leu Ile Lys Leu Ala Glu Asn Lys Thr Val 305 310 315 320 Ser Gly Ile Thr Asp Val Val Glu Asp Phe Val Thr Asp Val Ser Gln 325 330 335 Asn Ile Val Asp Lys Asn Lys Leu Phe Gly Thr Gly Thr Glu Ser Thr 340 345 350 Thr Gln Gly Leu Arg Lys Gln Val Ser Asn Thr Val Phe Lys Cys Leu 355 360 365 Thr Asn Gln Ile Asn Glu Gln Phe Asp Thr Ile Ser Asn Leu Glu Lys 370 375 380 Glu Arg Asp Asp Tyr Val Lys Lys Ile Gln Cys Ile Glu Thr Gln Leu 385 390 395 400 Leu Gln Ser Leu Pro Glu Gly Gly Arg Pro Arg His Asp Ile Asn Ile 405 410 415 Leu Thr Gln Asn Thr Leu Gln Ala Leu Ser Gly Leu Arg Asp Pro Thr 420 425 430 Ile Asn Leu Ser Glu Cys His Ile Pro Lys Gly Ser Ser Val Val Asn 435 440 445 Ser Phe Phe Ser Gln Tyr Val Pro Pro Phe Met Glu Met Leu Arg Glu 450 455 460 Leu Thr Ser Leu Trp Glu Gly Glu Met Phe Gln Thr Tyr Asn Leu Thr 465 470 475 480 Pro Val Val Asp Asn Gln Gly Gln Arg Thr Ser Ile Ala Tyr Ser Gln 485 490 495 Asp Thr Val Ser Ile Leu Leu Gly Pro Phe Thr Tyr Ile Ile Ala Lys 500 505 510 Leu Thr His Met Asp Leu Ile Asn His Ser Leu Ile Ser Leu Ser Leu 515 520 525 His Asp Ile Ala Asp Gln Leu Tyr Val Asp Ser Arg Leu Phe Val Tyr 530 535 540 Ile Asn Asp Ile Gly His Lys Tyr Cys Glu Gln Ile Ile Gln Pro Gly 545 550 555 560 Thr Asp Gly Pro Asn Thr Glu Ala Phe Asn Gly Gly Ala Ala Pro Ile 565 570 575 Gly Gly Asn Asn Ala 580 74 790 PRT Japanese Macaque Herpesvirus 74 Met Glu Ser Ser Val Gly Trp Thr Lys His Val Glu Pro Ser Pro Gly 1 5 10 15 Phe Ile Leu Asn Met Thr Ser Asp Ala Lys Val Arg Gly Val Val Asp 20 25 30 His Val Ser Arg Leu Ser Asn Ile Thr Thr Ser Pro Pro Glu Met Gly 35 40 45 Trp Tyr Asp Leu Ala Phe Asp Pro Ala Glu Asp Ser Gly Pro Phe Leu 50 55 60 Pro Phe Thr Val Tyr Leu Ile Thr Gly Thr Ala Gly Ala Gly Lys Ser 65 70 75 80 Thr Ser Ile Ser Ala Leu Tyr Gln Asn Leu Asn Cys Leu Ile Thr Gly 85 90 95 Ala Thr Thr Ile Ala Ala Gln Asn Leu Ser Arg Arg Leu Lys Thr Phe 100 105 110 Cys Pro Thr Ile Phe Ser Ala Phe Gly Phe Lys Ser Arg His Ile Asn 115 120 125 Ile Ala Val Arg Lys Ala His Gln Thr Gly Ala Val Ser Ile Glu Gln 130 135 140 Val Gln Gln Gln Glu Leu Ser Lys Tyr Trp Pro Val Ile Val Asp Ile 145 150 155 160 Met Lys Glu Val Met Ala Lys Lys Pro Asn Gly Met Tyr Gly Thr Ile 165 170 175 Ser Asn Ala Asp Phe Glu Thr Leu Ser Arg Met Thr Gly Pro Cys Leu 180 185 190 Trp Thr Ser Asn Ile Ile Val Ile Asp Glu Ala Gly Thr Leu Ser Ser 195 200 205 Tyr Ile Leu Thr Thr Val Val Phe Phe Tyr Trp Phe Leu Asn Ser Trp 210 215 220 Leu Asn Thr Pro Leu Tyr Arg Gln Gly Ala Val Pro Cys Ile Val Cys 225 230 235 240 Val Gly Ser Pro Thr Gln Thr Asn Ala Phe Gln Ser Thr Tyr Asn His 245 250 255 Gly Thr Gln Lys Thr Glu Ile Ser Ser Cys Glu Asn Ile Leu Thr Phe 260 265 270 Met Ile Gly Lys Lys Val Val Ser Glu Tyr Val Asn Leu Glu Arg Asn 275 280 285 Trp Ala Leu Phe Ile Asn Asn Lys Arg Cys Thr Asp Leu Gln Phe Gly 290 295 300 His Leu Leu Lys Ile Leu Glu Tyr Asn Leu Pro Ile Pro Asp Glu Val 305 310 315 320 Met Ser Tyr Val Asp Arg Phe Val Val Pro Lys Ser Lys Ile Met Asp 325 330 335 Pro Leu Glu Tyr Ile Gly Trp Thr Arg Leu Phe Leu Ser His Ser Glu 340 345 350 Val Lys Ala Tyr Leu Thr Asn Leu His Thr Cys Leu Thr Leu Gly Gly 355 360 365 Asp Thr Arg Asp Thr Lys Leu Phe Thr Cys Pro Val Val Cys Glu Val 370 375 380 Phe Val Lys Pro Phe Glu Glu Tyr Lys Arg Ala Val Asn Leu Thr His 385 390 395 400 Leu Thr Val Thr Glu Trp Val Thr Lys Asn Leu Phe Lys Leu Ser Asn 405 410 415 Tyr Ser Gln Phe Val Asp Gln Asp Met Ser Ile Val Ala Thr Glu Ser 420 425 430 Thr Glu Arg Ser Thr Gln Val Thr Phe Ile Thr Lys Phe Val Lys Asn 435 440 445 Ser His Val Ser Leu Asn Gly Lys Thr Lys Lys Cys Ile Cys Gly Phe 450 455 460 Gln Gly Thr Tyr Phe Glu Phe Lys Arg Ile Leu Asp Ser Glu Leu Phe 465 470 475 480 Val Glu Thr His Ser Gln Asp Arg Pro Glu Tyr Val Tyr Gly Phe Leu 485 490 495 Asn Thr Leu Leu Tyr Asn Ala Met Tyr Ser Phe His Ala Tyr Gly Val 500 505 510 Thr Arg Ala His Glu Lys Tyr Leu Glu Asp Leu Lys Phe Ala Pro Leu 515 520 525 Pro Thr Ala Leu Ala Thr Gly Arg Val Asp Phe Gln Thr Val Arg Glu 530 535 540 Glu Leu Asn Leu Glu Asp Asp Ile Phe Tyr His Val Cys Ser Pro Pro 545 550 555 560 Pro Pro Ala Gly Ile Thr Ser Leu Gln Val Leu Val Asp Thr Tyr Cys 565 570 575 Ala Leu Lys Asp Val Phe Ala Ser Arg Ile Lys Val Ala Cys Arg Trp 580 585 590 Phe Gly Gly Glu Phe Glu Lys Glu Thr Phe Ser Ala Phe Thr Val Asn 595 600 605 Met Val Val Arg Asp Gly Val Asp Phe Val Ser Pro Ser Glu Arg Leu 610 615 620 Asn Gly Leu Leu Ala Phe Ala Ser Thr Val Glu Ser Tyr Lys Ile Lys 625 630 635 640 Gly Tyr Thr Phe Leu Pro Ile Ala Phe Gly Arg Cys Gln Gly Leu Pro 645 650 655 Leu Ser Asp Asp Leu Arg Lys Lys Met Pro Ser Leu Val Val Gln Asp 660 665 670 Ser Ser Gly Phe Ile Ala Cys Leu Glu Asn Asn Ile Ser Lys Leu Thr 675 680 685 Glu Thr Met Asp Asp Gly Ser Val Phe Gln Val Cys Cys Ala Gly Asp 690 695 700 Tyr Gly Val Ser Ser Asn Leu Ala Met Thr Ile Val Lys Ala Gln Gly 705 710 715 720 Met Ser Leu Glu Arg Val Ala Val Val Phe Gly Ala His Lys Asn Val 725 730 735 Gln Thr Ser His Val Tyr Val Ala Ile Ser Arg Ala Val Asn Ser Asn 740 745 750 Tyr Leu Val Met Asp Ser Asn Pro Leu Lys Thr Leu Leu Arg Glu Pro 755 760 765 Val Asp Asn Thr Ser Ala Lys His Ile Val Arg Ala Leu His Asn Pro 770 775 780 Asn Thr Thr Leu Ile Tyr 785 790 75 137 PRT Japanese Macaque Herpesvirus 75 Met Val Ser Val Ser Leu Asp Met Leu Phe Ser Arg His Ala Ile Lys 1 5 10 15 Pro Leu Glu Ser Cys Thr Thr Arg Asp Gly Ile Phe Phe Leu Arg Ser 20 25 30 Ser Leu Ser Gly Asn Pro Trp Gln Arg Pro Asn Ala Ile Gly Lys Asn 35 40 45 Val Tyr Pro Leu Ile Leu Tyr Asp Ser Thr Val Asp Ala Asn Ala Asn 50 55 60 Asn Pro Phe Arg Arg Ser Glu Gly Glu Thr Lys Ser Thr Pro Ser Leu 65 70 75 80 Thr Thr Met Leu Thr Val Asn Ala Glu Asn Val Ser Phe Ser Asn Ser 85 90 95 Pro Pro Asn Gln Arg His Ala Thr Phe Ile Leu Glu Ala Asn Thr Ser 100 105 110 Phe Arg Ala Gln Tyr Val Ser Thr Lys Thr Trp Arg Glu Val Ile Pro 115 120 125 Ala Gly Gly Gly Gly Leu His Thr Trp 130 135 76 353 PRT Japanese Macaque Herpesvirus 76 Met Ala Met Phe Leu Ser Asp Pro Pro Arg Thr Pro Pro Ala Thr Pro 1 5 10 15 Arg Met Leu Pro Ile Pro Gly Ala Pro Arg Lys Lys Arg Thr Arg Arg 20 25 30 Phe Leu Phe Ala Gly Ser Arg Thr Gly Leu Pro Val Pro Pro Gly Tyr 35 40 45 Gly Gly Pro Pro Val Ile Asp Met Thr Ala Pro Asn Asp Val Phe Asp 50 55 60 Ala Asp Ser Pro Pro Thr Thr Pro Lys Thr Pro Asp Glu Thr Asp Ser 65 70 75 80 His Ser Glu Asn Ser Asn Tyr Ser Asp Met Asp Glu Glu Asp Glu Gln 85 90 95 Pro Val Ser Ser Pro Pro Arg Ile Asp Pro His Ala Arg Asp Gly Glu 100 105 110 Ser Phe Asn Gln Ser Asp Trp Arg Pro Thr Val Ile Thr Ala Ala Gly 115 120 125 Pro Ala Ala Gln Pro Ser Ala Pro Ala Pro Leu Thr Ala Phe Gly Gly 130 135 140 Gln Arg Pro Val Ala Val Val Thr Gly Gln His Arg Ala Pro Pro Ser 145 150 155 160 Ser Thr Ser Asp Ser Gly Asp Asp Phe Phe Ile Asp Asp Tyr Glu Asp 165 170 175 Thr Asp Glu Ser Gly Glu Asp Ala Asp Gly Phe Ser Pro Arg Ala Ser 180 185 190 Pro Ala Trp Ser Gly Asp Thr Ser Arg Ser Pro Ala Gly Gly Gly Trp 195 200 205 Ser Ser Asn Glu Glu Glu Glu Pro Ala Val Thr Gly Ser Ala Val Glu 210 215 220 Gln Glu Thr Ile Ile Ile Ser Asp Asp Asp Asp Thr Asp Asp Arg Gly 225 230 235 240 Ser Val Glu Thr Trp Asp Glu Ser Asp Ala Asp Glu Gly Thr Gly Ala 245 250 255 Thr Asp Val Ile Asp Leu Cys Ser Ser Ser Asp Ser Asp Asp Asp Ala 260 265 270 Asp His Val Thr Ser Gly Gly Val Arg Ala Ala Cys Lys Arg His Ala 275 280 285 Ser Arg Arg Asp Cys Asn Gly Asp Asp Asp Val Ile Tyr Leu Gly Thr 290 295 300 Thr Arg Ala Pro Lys Arg Arg Met Thr Ser Thr Thr Gly Gly Gly Ala 305 310 315 320 Thr Ser Asn Pro Glu Gly Pro Gly Val Ser Gly Arg Gln Thr Met Ala 325 330 335 Ala Thr Pro Pro Val Cys Gly Asn Asp Asn Tyr Pro Trp Pro Trp Leu 340 345 350 Asp 77 87 PRT Japanese Macaque Herpesvirus 77 Met Arg Val Gly Phe Val Trp Arg Phe Trp Ser Gly Gly Arg Arg Ile 1 5 10 15 Cys Ile Lys Asn Ile Val Arg Cys Ser His Val Asn His Arg Gly Ala 20 25 30 Ser Val Thr Gly Arg Tyr Arg Gln Pro Arg Thr Gly Pro Gly Glu Gln 35 40 45 Lys Pro Ser Cys Ser Leu Phe Pro Arg Cys Thr Gly Asn Arg Gln His 50 55 60 Pro Gly Ser Gly Arg Arg Gly Pro Trp Arg Val Arg Gln Glu His Ser 65 70 75 80 His Asp Gln Asn Val His Leu 85 78 255 PRT Japanese Macaque Herpesvirus 78 Met Asp Thr Trp Leu Glu Thr Val Val Trp His Lys Met Ser Met Thr 1 5 10 15 Gly Pro Asn Glu Thr Pro Thr Gln Met Leu Leu Ile Ser Asp Ser Trp 20 25 30 Leu Lys Phe Leu Asn Leu Ser Pro Phe Leu Lys Lys Lys Leu Ala Ala 35 40 45 Leu Leu Arg Arg Val Met Asp Met Ser Lys Ala Thr Val Ile Tyr Pro 50 55 60 Pro Ile Asp Arg Ile Met Trp Trp Ser Tyr Cys Cys Glu Pro Glu Asp 65 70 75 80 Ile Lys Val Val Ile Leu Gly Gln Asp Pro Tyr His Arg Gly Gln Ala 85 90 95 Thr Gly Leu Ala Phe Ser Val Ala Pro Asp Tyr Ser Ile Pro Pro Ser 100 105 110 Leu Lys Asn Ile Phe Lys Glu Ile Ala Asn Thr Val Pro Gly Phe Thr 115 120 125 Ala Pro Ser His Gly Cys Leu Asp Cys Trp Ala Lys Arg Gly Val Leu 130 135 140 Leu Leu Asn Thr Ile Leu Thr Val Glu Arg Gly Lys Ala Gly Ser His 145 150 155 160 Ser Asn Leu Gly Trp Asp Trp Phe Thr Ser Tyr Ile Ile Ser Cys Leu 165 170 175 Ser Ala Lys Leu Gln Arg Cys Val Phe Met Leu Trp Gly Arg Lys Ala 180 185 190 Ile Asp Lys Ala Val Leu Ile Asn Gly Gln Arg His Leu Val Leu Lys 195 200 205 Ala Arg His Pro Ser Pro Leu Ala Ala Ala His Ala Ala Thr Gly Ser 210 215 220 Pro Trp Pro Gln Phe Leu Gly Cys Asn His Phe Lys Leu Ala Asn Asp 225 230 235 240 Tyr Leu Val Gln Asn Gln Arg Gly Ala Val Asp Trp Asn Ile Asn 245 250 255 79 163 PRT Japanese Macaque Herpesvirus 79 Met Tyr Thr Leu Ser Phe Phe Thr Thr Tyr Phe Ile Leu Tyr Ile Gly 1 5 10 15 Tyr Ser Ser Gly Leu Ile Pro Asn Pro Cys Cys Asp Ile Val Pro Leu 20 25 30 Thr Gly Val Asn Ile Pro Ala Pro Phe Glu Ile Val Ser Phe His Phe 35 40 45 Thr Asp Leu Ala Trp Cys Gln Gly Arg Cys Val Ala Thr Leu Arg Tyr 50 55 60 Lys Val Gly Thr Ile Thr Thr Glu Leu Cys Val Asn Gly Phe His Leu 65 70 75 80 Arg Ala Phe Phe Ile Arg Ile Leu Ser Gly Leu Asp Phe Ser Val His 85 90 95 Arg Glu Glu Leu Asp Leu Leu Asn Tyr Val Arg Ile Ser Leu Glu Asp 100 105 110 Phe Leu Ser Ala Phe Lys Asp Thr His Asp Asn Ser Glu Ser Val Thr 115 120 125 Asn Leu Pro Ala Val Pro Asp Leu Thr Lys Lys Gly Ser Ala Ala Phe 130 135 140 Arg Thr Arg Lys Val Gly Ala Arg Arg Gly Asp Leu Trp Ile Leu Gly 145 150 155 160 Ser Arg Gln 80 389 PRT Japanese Macaque Herpesvirus 80 Met Ala Val Ser Ile Pro Val Gln Gly Val Asp Arg Glu Thr Glu Ser 1 5 10 15 Asn Trp Arg Ser Ile Val Thr Thr Phe Glu Gln His Gly Asn Ala Asp 20 25 30 Arg Ala Ile Arg Ser Leu Leu Arg Phe Phe Lys Gly Val Asp His Pro 35 40 45 Gly Phe Leu Ala Ser Leu Val Ile Leu Lys Asp Val Ala Ile Asp Ser 50 55 60 Glu Lys Thr Ile Glu Arg Thr Asp Ile Ile Pro Leu Leu Gln Gly Val 65 70 75 80 Arg Phe Val Thr Gln Gln Ile Tyr Met His Leu Lys Asp His Ala Ser 85 90 95 Glu Ser Pro Val Thr Glu Ile Trp Arg Asp Cys Lys Glu Arg Phe Cys 100 105 110 Leu Ala Leu Glu Leu Ala Cys Gly Cys Gln Ser Cys Thr Ser Ala Ala 115 120 125 Arg Gln Leu Arg Asp Cys Gln Gln Ala Cys Arg Pro Pro Lys Leu Asn 130 135 140 Pro His Lys Gln Gln Cys Gly Ala Ala Arg Leu Leu Thr Ala Val Tyr 145 150 155 160 Asn Gln Met Val Leu Arg Thr Arg Val Ser Val Ser Glu Phe Cys Leu 165 170 175 Asn Ala Leu Met Cys Val Pro Arg Glu Phe Gly Phe Val Ser Gly Asp 180 185 190 Val Arg Val Glu Thr Ser Arg Val Ala Ser Cys Met Asn Leu Ser Trp 195 200 205 Leu Tyr Leu Ile Leu Asp Ser Tyr Ile Arg Thr Asp Leu Thr Asn Leu 210 215 220 Glu Met Ala Met Ser Arg Ala Cys Arg Ile Arg Gly Leu Ser Thr Arg 225 230 235 240 Asp Pro Phe Tyr Ser Ala Leu Val Trp Leu Lys Asn Ser Cys Ala Cys 245 250 255 Ala Ala Asn Thr Phe Phe Phe Thr Val Asn Ser Thr Arg Val Thr Thr 260 265 270 Pro Ile Leu Met Asp Ile Cys Ala Ser Leu Ala Gly Pro Val Pro Asp 275 280 285 Val Ile Lys Ile Asn Met Leu Pro Leu Val Asn Asn Gln Met Tyr Pro 290 295 300 Ser Val Cys Val Glu Arg Ala Asn Phe Thr Gly Ser Cys Pro Lys Met 305 310 315 320 Ser Pro Thr His Arg Phe Asp Gly Leu Lys Leu Glu Thr Thr Ser Leu 325 330 335 Thr Leu Ala Ala Asp Ser Leu Asp Asp Ile Leu Gln Ala Leu Glu Leu 340 345 350 Ile Cys Asp Asp Asp Glu Gly Ile Leu Asp Ser His Ile Ser Asp Ile 355 360 365 Asp Thr Glu Thr Glu Val Asp Glu Ser Thr Ile Glu Glu Glu Ile Val 370 375 380 Phe Glu Glu Leu Ser 385 81 83 PRT Japanese Macaque Herpesvirus 81 Met Val Asp Pro Phe Lys Lys Ser Gln Lys Arg Pro Asp Gly Ser Ile 1 5 10 15 Arg Val Ser Met Leu Phe Lys Gly Ser His Asp Gly Ser Pro Val Arg 20 25 30 Leu Gly Leu Pro Val Asn Thr Leu Asn Trp Asn Gly Asn Ser His Asp 35 40 45 Thr Val Asn Phe Leu Met Ser Pro Lys Thr Asn Pro Glu Thr Glu Leu 50 55 60 Asn Thr Asn Asp Cys His Pro Tyr Pro Lys Pro Arg Pro Arg Thr Ile 65 70 75 80 Arg Pro Gly 82 81 PRT Japanese Macaque Herpesvirus 82 Met Asp Thr Asp Asp Asn Gln Val Ile Lys Leu Phe Phe Ile Gln Asp 1 5 10 15 Ser Gly Gly Arg Val Tyr Ser Gly Val Gly Gly Ser Ile Ser Arg Arg 20 25 30 Trp Glu Trp Leu Met Asn Pro His Leu Val Leu Gly Ser Gly Ala Leu 35 40 45 Cys Ile Leu Leu Val Gln Leu Asn Leu Asn Leu Ala Cys Leu Gly Arg 50 55 60 Thr Asn Gln Lys Thr Ala Trp Pro Arg Leu Leu Gly Ala Leu Cys Lys 65 70 75 80 Leu 83 301 PRT Japanese Macaque Herpesvirus 83 Met Ser Arg His Tyr Gly Lys Asp His Leu Leu Asn His Met Tyr Lys 1 5 10 15 Phe His Tyr Pro Pro Leu Gly Met Ile Val Gly Glu Met Asn Thr Leu 20 25 30 Thr Val Asn Ala Arg Asn Pro Leu Tyr Gln Ala Ala Thr Leu Arg Val 35 40 45 Glu Arg Ala Leu Tyr Leu Ser Lys Ile Leu Gln Val Leu Met Gln His 50 55 60 Arg Gln Gly Glu Arg Phe Ile Val Pro Gln Cys Arg Ser Asn Met Val 65 70 75 80 Tyr Cys Leu Lys Glu Leu His Lys Ile Thr Asn Asp Arg Ile Arg Gly 85 90 95 Leu Ile Asn Ser Val Leu Pro Leu Val Asp Ala Gly Cys Val Gly Phe 100 105 110 Asp Glu Glu Leu Val Arg Ile Leu Pro Glu Ile Leu Lys Leu Glu Tyr 115 120 125 Pro His Val His Glu Leu Leu Pro Pro His Asp Pro Thr Ser Pro Leu 130 135 140 Ser Trp Cys Leu Ser His Met Val Gly Val Thr Lys Thr Phe Lys Gly 145 150 155 160 Glu Val Lys Glu Met Ile Asp Thr Phe His Asp Leu Ser Val Pro Ser 165 170 175 Phe Gln Tyr Leu Ala Ser Leu Val Lys Lys Phe Phe Leu Val Glu Glu 180 185 190 Val Ile Tyr Glu Asp Tyr Gln Asp Thr Gln Phe Asn Val Phe Leu Asn 195 200 205 Leu Cys Phe Phe Trp Thr Thr Val Ile Lys Met Tyr Gln Ser Cys Ile 210 215 220 Phe Lys Asp Lys Leu Leu Asp Thr Ile Lys Ala Cys Ile Glu Leu Leu 225 230 235 240 Lys Gly Glu Ala Arg Gln Phe Phe Gly Trp Tyr Asp Leu Asn Thr Pro 245 250 255 Asn Leu Gly Ser Ala Ala Leu Val Lys Tyr Thr Glu His Leu Ile Arg 260 265 270 Ala Leu Ser Val Asp Ser Ser Ala Ile Pro Ile Gly Glu Ile Cys Ser 275 280 285 His Leu His His Cys Lys His Ala Leu Leu Asn Leu Glu 290 295 300 84 85 PRT Japanese Macaque Herpesvirus 84 Met Gly Met Ala Asp Glu Ser Thr Leu Ser Ala Arg Ile Arg Cys Ser 1 5 10 15 Val Tyr Phe Thr Ser Ala Ala Glu Pro Lys Phe Gly Val Phe Arg Ser 20 25 30 Tyr Gln Pro Lys Asn Cys Leu Ala Ser Pro Phe Arg Ser Ser Met Gln 35 40 45 Ala Leu Met Val Ser Asn Ser Leu Ser Leu Lys Met Gln Leu Trp Tyr 50 55 60 Ile Phe Met Thr Val Val Gln Lys Lys Gln Arg Phe Lys Asn Thr Leu 65 70 75 80 Asn Cys Val Ser Trp 85 85 514 PRT Japanese Macaque Herpesvirus 85 Met Glu Cys Ala Ser Leu Gly Pro Ile Ser Gly Leu Ile Ala Asp Leu 1 5 10 15 Asn Leu Phe Asn Leu Phe Cys Leu Tyr Arg Gly Ser Arg Val Lys Thr 20 25 30 Arg Gly Ala Ala Thr Cys Asn Val Pro Cys Ala Glu Cys Ala Gln Gly 35 40 45 Val Val Arg Ile Leu Thr Glu Arg Ala Leu Cys Cys Thr Glu Lys Met 50 55 60 Phe Ile Ala Ser Ala Cys Ser Gly Val Val Leu Pro Pro Gln Leu Ala 65 70 75 80 Lys Val Phe His Asp Val Tyr Ala Glu Met Lys Ala Lys Cys Leu Gly 85 90 95 Ala Trp Arg Arg Leu Ile Cys Cys Arg Arg Pro Ile Met Ala Ile Ala 100 105 110 Asp Ser Val Leu Val Thr Tyr Asn Thr Leu Asp Ala Glu Gly Lys Leu 115 120 125 Asp Leu Lys Leu Lys Ala Leu Cys Lys Leu Val Phe Gln Pro Ile Phe 130 135 140 Leu Gln Arg Ile Leu Ala Pro Met Gln Leu Leu Ala Asn Gly Lys Met 145 150 155 160 Val Pro Asp Asn Tyr Phe Thr Ile Thr Gly Thr Ala Glu Lys Arg Arg 165 170 175 Pro Val Val Thr Gly Ser Thr Ser Gly Met Thr Cys Pro Gly Ser Ser 180 185 190 Leu Val Pro Asp Ser Leu Ile Leu Pro Val Cys Glu Pro Gly Leu Leu 195 200 205 Pro Ala Pro Leu Val Asp Leu Ser Asn Val Leu Glu Asn Pro Glu Ile 210 215 220 Ile Leu Ser Ala Pro Pro Leu Ser Gln Phe Val Ile Thr Asn Thr His 225 230 235 240 Pro Ser Leu Pro Gln Ser Val Ser Ile Ile Thr Pro Thr Gln Gly Val 245 250 255 Val Pro Gly Gln Cys Phe Met Asp Thr Trp Lys Ala Val Ser Gln Ser 260 265 270 Ile His His Gln Ala His Thr Pro Ile Phe Ala Ala Thr Leu Ala Gly 275 280 285 Ser Thr Ser Ala Ala Pro Gly Pro His Ile Ala Cys Ser Pro Val Ala 290 295 300 Gly Thr Ser Arg Gln Val Glu Ala Ser Ala Gly Val Asp Cys Gly Lys 305 310 315 320 Pro Val Cys Ala Pro Gln Pro Asp Ile Pro Pro His Val Pro Thr Lys 325 330 335 Arg Met Glu Thr Val Ala Gln Ser Gly Asn Ala Pro Val Lys Asn Val 340 345 350 His Ile Gly Gly Arg Val Tyr Ala Pro Leu Val Asn Ile Pro Ile Ile 355 360 365 Asp Leu Thr Ser Pro Ser Gly Ser Gly Gln Ser Pro Val Asn Ile Ala 370 375 380 Asn Thr Pro Glu Ser Arg Met Ala Ala Gly Ser Pro Pro Phe Ala Glu 385 390 395 400 Thr Ala Ala Thr Val Pro Ala Lys Arg Lys Gln Pro Arg Glu Asp Val 405 410 415 Ala Asp Lys Arg Ser Lys Gly Asp Gly Arg Gly Ala Ala Thr Val Asn 420 425 430 Pro Pro Phe Pro Gly Pro Pro Ala Met Arg Val Arg Glu Gln Gly Leu 435 440 445 Phe Asp Leu Ile Glu Ser Ser Thr Asp Val Thr Ala Asn Ala Ser Gly 450 455 460 Pro Lys Asn Asp Asp Asp Met Leu Ala Ala Ile Leu Gln Asp Leu Tyr 465 470 475 480 Gly Leu Gln Ser Pro Pro Ala Ile Asp Ser Pro Ser Ser Asn Ser Asp 485 490 495 Asn Glu Asp Ile Phe Pro Glu Val Ser Pro Pro Ser Ser Gly His Gly 500 505 510 Ser Pro 86 224 PRT Japanese Macaque Herpesvirus 86 Met Ser Ser Leu Ser Glu Leu Leu Glu Gly Glu Ser Ile Ala Gly Gly 1 5 10 15 Asp Cys Arg Pro Tyr Arg Ser Cys Arg Ile Ala Ala Asn Met Ser Ser 20 25 30 Ser Phe Phe Gly Pro Asp Ala Phe Ala Val Thr Ser Val Glu Leu Ser 35 40 45 Ile Lys Ser Asn Lys Pro Cys Ser Arg Thr Arg Ile Ala Gly Gly Pro 50 55 60 Gly Asn Gly Gly Phe Thr Val Ala Ala Pro Arg Pro Ser Pro Phe Asp 65 70 75 80 Leu Leu Ser Ala Thr Ser Ser Arg Gly Cys Phe Leu Leu Ala Gly Thr 85 90 95 Val Ala Ala Val Ser Ala Lys Gly Gly Glu Pro Ala Ala Met Arg Asp 100 105 110 Ser Gly Val Leu Ala Ile Leu Thr Gly Leu Cys Pro Glu Pro Asp Gly 115 120 125 Asp Val Lys Ser Ile Ile Gly Ile Leu Thr Ser Gly Ala Tyr Thr Arg 130 135 140 Pro Pro Met Trp Thr Phe Phe Thr Gly Ala Phe Pro Asp Cys Ala Thr 145 150 155 160 Val Ser Ile Leu Leu Val Gly Thr Trp Gly Gly Ile Ser Gly Cys Gly 165 170 175 Ala His Thr Gly Phe Pro Gln Ser Thr Pro Ala Asp Ala Ser Thr Cys 180 185 190 Arg Asp Val Pro Ala Thr Gly Glu His Ala Ile Cys Gly Pro Gly Ala 195 200 205 Ala Asp Val Glu Pro Ala Ser Val Ala Ala Lys Ile Gly Val Cys Ala 210 215 220 87 170 PRT Japanese Macaque Herpesvirus 87 Met Pro Arg Val Lys Thr Gln Pro Lys Arg Pro Gln Val Phe Asp Phe 1 5 10 15 Met Pro Leu Asp Leu His Gly Glu Thr Arg Ala Glu Met Asp Ser Gln 20 25 30 Ser Leu Cys Pro Asp Gly Gln Asp Leu Leu Gly Ser Tyr Ile Tyr Thr 35 40 45 Glu Asn Asn Gly Pro Phe Ser Gln Met Met His Asn Gly Gln Ser Asn 50 55 60 Asn Gly Thr Gly Glu Ser Phe Gly Ser Tyr Ala Ala Gly Asp Gly Phe 65 70 75 80 Leu Gly Gly Ser Val Ser Gly Met His Gly Asn Gly Thr Val Asp Gly 85 90 95 Leu Cys Ser Lys Lys Gln Ser Ala Cys Arg Lys Arg Ser Ala Ala Leu 100 105 110 Ile His Ala Ala Ser Glu Ala Ser Val Ala Glu Gln Gly Thr Ser Gln 115 120 125 Gly Thr Asn Ala Val Ser Asp Arg Ile Gly Arg Asp Gly Gly Ile Gly 130 135 140 Asn Lys Leu Leu Lys Val Ser Ala Arg Leu Pro Asp Lys Thr Lys Thr 145 150 155 160 Leu Pro Asp Pro Ser Leu His Cys Tyr Phe 165 170 88 244 PRT Japanese Macaque Herpesvirus 88 Met Arg Ile Tyr Gly Ile Lys Gly Leu Asn Phe Phe Gly Ile Met Gly 1 5 10 15 Phe Trp Asn Ile Pro Leu Gly Trp Gly Leu Cys Phe Met Val Trp Val 20 25 30 Ala Trp Ile Ala Arg Gly Arg Ser Val Cys Pro Thr Trp His Leu Thr 35 40 45 Asp Gly Lys Tyr Glu Ala Val Tyr Arg His Tyr Leu Glu Glu Cys Arg 50 55 60 Lys His Glu Gly Ser Gly Ser Pro Asp Gly Ser Gly Lys Thr Glu Gly 65 70 75 80 Ser Gly Thr Lys Ala Thr Thr Glu Ala Asn Ile Ser Ile Arg Pro Asn 85 90 95 Val Val Thr Ser Gly Gln Asp Lys Glu Pro Met Lys Thr Ala Pro Arg 100 105 110 Ala Glu Ser Ser His Asp Leu Pro Arg Ile Glu Gln Val Asn Ala Leu 115 120 125 His Leu Ser Thr Pro Glu Leu Ala Gln Pro Leu Pro Val Val Glu Ser 130 135 140 Thr Pro Arg Glu Ser Gln Ser Gly Gly Thr Pro Trp Asp Ala Arg Pro 145 150 155 160 His Ala Phe Ile Met His Thr Asn Asp Met Leu Asn Pro Ser Val Val 165 170 175 Leu Ser Phe Arg Ala Val Arg Ala Arg Ser Ile Arg Asp Thr Glu Gln 180 185 190 Ser Ile Arg Asp Arg Asn Thr Val Thr Thr Ser Tyr Arg Thr Pro Gly 195 200 205 Arg Pro Ser Leu Val Gln Ala Arg Pro Ser Ser Tyr Gly Ala Arg Leu 210 215 220 Pro Pro Ser Pro Arg Thr Met Ala Arg Tyr Ala Glu Thr Arg Pro Thr 225 230 235 240 Asp Asp Gln Asn 89 92 PRT Japanese Macaque Herpesvirus 89 Met Asp Cys Ser Val Ser Arg Met Glu Arg Ala Arg Thr Ala Leu Lys 1 5 10 15 Asp Arg Thr Thr Asp Gly Leu Ser Met Ser Phe Val Cys Ile Met Asn 20 25 30 Ala Trp Gly Arg Ala Ser Gln Gly Val Pro Pro Asp Cys Asp Ser Arg 35 40 45 Gly Val Asp Ser Thr Thr Gly Arg Gly Cys Ala Asn Ser Gly Val Asp 50 55 60 Lys Trp Arg Ala Leu Thr Cys Ser Met Arg Gly Arg Ser Cys Asp Asp 65 70 75 80 Ser Ala Leu Gly Ala Val Phe Ile Gly Ser Leu Ser 85 90 90 139 PRT Japanese Macaque Herpesvirus 90 Met Ser Ser Thr Arg Pro Lys Thr Arg Ala Pro Lys Lys Glu Leu Thr 1 5 10 15 Met Glu Glu Leu Ala Ala Gln Val Gln Lys Leu Ser Val Glu Asn Lys 20 25 30 Gln Leu Lys Lys Leu Ile Asn Ser Gly Asp Pro Thr Arg Ser Gly Ser 35 40 45 Asp Pro Val Ile Ser Asn Ser Glu Lys Glu Ala Lys Ile Ala Ala Ala 50 55 60 Val Ser Ala Leu Cys Asn Val Ala Thr Arg Lys Ile Glu Ala Lys Val 65 70 75 80 Arg Ala Val Thr Ala Lys Ala Val Thr Arg Gly Gln Val Glu Glu Ala 85 90 95 Leu Ala Gly Ile Asn Ile Arg Val Asp Val Ser Met Asp Glu Thr Thr 100 105 110 Arg Gly Gly Ile Thr Ala Ser Ala Asp Gly Ala Leu Arg Arg Arg Arg 115 120 125 Ala Gln Ser Arg Thr Arg Asn Asn Asp Ala Asp 130 135 91 104 PRT Japanese Macaque Herpesvirus 91 Met Thr Gly Ser Ile Val Leu Ala Leu Ala Leu Thr Ala Cys Leu Tyr 1 5 10 15 Leu Cys Leu Pro Val Cys Ala Thr Val Thr Thr Ser Ser Thr Thr Gly 20 25 30 Thr Gly Thr Pro Pro Val Thr Thr Thr Pro Ser Ala Ala Pro Ser Val 35 40 45 Thr Pro Ser Phe Tyr Asp Tyr Asp Cys Ser Ala Asp Thr Tyr Gln Pro 50 55 60 Val Leu Ser Ser Phe Ser Ser Ile Trp Ala Val Ile Asn Ser Val Leu 65 70 75 80 Val Ala Val Ala Thr Phe Leu Tyr Leu Thr Tyr Met Cys Phe Phe Lys 85 90 95 Phe Val Glu Thr Val Ala His Glu 100 92 290 PRT Japanese Macaque Herpesvirus 92 Met Ala Glu Val Thr Ala His Thr Val Ala Tyr Ala Phe Asp Ser Cys 1 5 10 15 Lys Phe Glu Ile Ile Pro Lys Asn Asn Ser Ser Arg Ile Ala Leu Arg 20 25 30 Asn Lys Phe Pro Val Val Val Lys Pro Gly Glu Pro Leu Val Val Pro 35 40 45 Leu Gly Leu Arg Ile Ile Arg Ala Pro Gln Cys Ala Phe Phe Leu Ser 50 55 60 Gly Ala Pro Thr Asp Glu Val Tyr Tyr His Thr Gly Leu Ile Asp Gln 65 70 75 80 Gly Tyr Arg Gly Glu Ile Lys Leu Ile Val Leu Asn Lys Thr Lys Gln 85 90 95 Ser Val Thr Leu Tyr Arg Gly Glu Val Asn Val Ser Leu Ile Ala Phe 100 105 110 Met Tyr Ala Ser Pro Gly Pro Leu Lys Cys Pro Ile Leu Asn Leu Pro 115 120 125 His Tyr Ser Leu Asp Ala Gly Phe Asp Val Thr Ser Pro His Ala Met 130 135 140 Thr Ile Pro Pro Thr Asp Arg Thr Pro Phe Thr Leu Ser Leu Tyr Tyr 145 150 155 160 Lys Ser Pro Gln Leu Ser Thr Pro His Val Pro Leu Ile Val Gly Arg 165 170 175 Ser Gly Leu Ala Ala Lys Gly Leu Thr Val Asp Ala Thr Lys Trp Thr 180 185 190 Gln Ser Leu Val His Leu Arg Phe Tyr Asn Phe Thr Lys Glu Pro Ile 195 200 205 Asp Ile Pro Ala Asn Ser Arg Ile Cys Gln Val Val Phe Ile His Glu 210 215 220 Asp His Val Pro Ser Gly Trp Asn Ile Leu Arg Ser Arg Val Gln Leu 225 230 235 240 Gly Ser Thr Leu Gln Ile Ser Trp Ala Lys Ile Arg Phe Thr Asp Val 245 250 255 Ala Thr Leu Pro Ala Thr His Pro Leu Asn Ser Arg Pro Thr Gln Ser 260 265 270 Gln Thr Glu Pro Glu Thr Asn Arg Gly Ala Lys Gly Leu Gly Ser Ser 275 280 285 Gly Leu 290 93 140 PRT Japanese Macaque Herpesvirus 93 Met Ser Gly Ser Val Tyr Ser Arg Arg Pro Arg Pro Lys Arg Val Glu 1 5 10 15 His Ser Glu Ile Pro Arg Thr Thr Arg Gln His Pro Pro Asp Ile Val 20 25 30 Gly Gln Asn Gln Val His Arg Arg Gly His Ala Ser Arg Asn Pro Pro 35 40 45 Ala Gln Leu Pro Pro His Ser Lys Pro Asp Arg Thr Arg Asp Gln Pro 50 55 60 Arg Arg Lys Gly Val Gly Val Val Arg Val Ile Ile Leu Lys His Gly 65 70 75 80 Ile Ile Leu Lys Leu Phe Ile Phe Asn Lys Thr Ile Gln Ile Asn Ile 85 90 95 Asn His Gln Pro Gly His Leu Val Leu Phe Cys Leu Ala Arg Tyr Tyr 100 105 110 Pro Pro Pro Pro Thr Gly Ala Ser Val Val Glu Ser Pro Asp Gly Arg 115 120 125 Gly Trp Arg Thr Leu Arg Tyr Leu Pro Ala His Tyr 130 135 140 94 210 PRT Japanese Macaque Herpesvirus 94 Met Ala Ala Pro Gly Ser Phe Trp Thr Cys Cys Gly Phe Ser Pro Phe 1 5 10 15 Gly Arg Val Gly Cys Arg Tyr Arg Pro Leu Pro Asp Pro Leu Asn Glu 20 25 30 Cys Pro Thr His Trp Arg Thr Glu Ile Ala Met Gly Leu Pro Pro Gly 35 40 45 Val Asp Met Gly Asp Val Lys Gln Ala Glu Met Cys Thr Ala Ala Leu 50 55 60 Arg Gln Thr Tyr Leu Leu Ala Val Gln Ser Asn Lys Ile Thr Glu Tyr 65 70 75 80 Leu Arg Arg Phe Asp Ala Ala Arg Val Pro Ala Gly Cys Gln Glu Thr 85 90 95 Val Arg Ile Gln Ile Ser Lys Leu Lys Ser Ile Gln Asn Val Ile Trp 100 105 110 Asn Ala Met Leu Ser Leu Ala Ile Gly Asp Ile Thr Val Asp Glu Ser 115 120 125 Ala Phe His Ala Leu Leu Asn Lys Arg Ala Asp Glu Thr Val Ser Leu 130 135 140 Leu Glu Met Glu Lys Leu Ala Thr Thr Ile Ala Ser Asp Asp Ser Val 145 150 155 160 Thr Trp Ala Ala Glu Ile Asn Asn Val Leu Val Asp Thr Glu Ala Ser 165 170 175 Ser Asn Pro Ser His Pro Val Ile Arg Gln Pro Thr Pro Gln Leu Ala 180 185 190 Val Ala Asp Asn Ile Val Pro Asp Lys Ile Ile Gln Asp Ala Gln Ala 195 200 205 Asp Gly 210 95 838 PRT Japanese Macaque Herpesvirus 95 Met Ser Gln Val Arg Pro Leu Pro Asp Glu Arg Val Asn Glu Ile Arg 1 5 10 15 Ala Ile Phe Ser Thr Ser Gly Asp Met Ala Glu Val Ile Thr Asp Ile 20 25 30 Leu Thr Gly Thr Gln Ala Thr Ala Ser Phe Phe Cys Val Leu His Asp 35 40 45 Arg Gly Asn Val Pro Ile Asn Thr Pro His Ala Val Ile Lys Leu Cys 50 55 60 Leu Pro Ala Arg Arg Pro Gly Gly Gly Pro Arg Cys Leu Pro Leu Met 65 70 75 80 Val Leu Asn Leu Pro Ala Trp Gln Val His Leu Phe Leu Thr Gly Asp 85 90 95 Ala Pro Leu Thr Ser Asp Asn Ile Lys Asp Arg Ile Asp Leu Ala Gln 100 105 110 Thr Glu Glu Ile Leu Glu Pro Ile Leu Ser Val Leu Ala Cys Lys Arg 115 120 125 Ser Ala Gln Gln Thr Lys His Asp Ser Phe Lys Ser Lys Val Ala Trp 130 135 140 Phe Arg Ala Lys Phe Val Ser Ala Leu Arg Lys Val Tyr Lys Met Thr 145 150 155 160 Pro Ser Pro Tyr Trp Met Ile Thr Leu Leu Gly Ser Phe Glu Ala Ser 165 170 175 Phe Val Leu Ala Gly Thr Phe Tyr Phe Phe Gln Ser Tyr Thr Cys Thr 180 185 190 Ala Glu Thr Leu Val His Leu Thr Arg Leu Phe Ile Ser Ser Gln Gly 195 200 205 Gln Ser Leu Val Thr Val Asn Thr Tyr Asp Glu Leu Gly Arg Val Phe 210 215 220 Gly Arg Ser Asp Phe Leu Glu Ile Val Pro Asn Phe Trp Ala Tyr Leu 225 230 235 240 Lys Tyr Lys Met Gln Gln Asp Asp Val Glu Ser Lys Ala Ile Asp Gln 245 250 255 Thr Ile Asn Ser Ile Arg Gly Gly Leu Met Leu Ser Pro Gln Asp Leu 260 265 270 Val His Phe Ile Tyr Leu Ser Phe Tyr Glu Cys Met Asn Ala Gln Thr 275 280 285 Phe Leu Ser Tyr Ser Arg Thr Thr Ala Ser Leu Pro Thr Pro Ala Thr 290 295 300 Val Asn Pro Pro Gln Leu Cys Arg Arg Leu Glu Ala Asp Phe Lys Glu 305 310 315 320 His Val Met Ala Tyr Tyr Asn Lys Ala Ser Tyr Leu Ser Thr Tyr Ile 325 330 335 Thr Ile Leu Thr Val Pro Ala Pro Leu Pro Glu Gly Tyr Glu Asn Phe 340 345 350 Gln Glu Leu Ala Cys Gln Tyr Trp Cys Gly Gln Ser Arg Asp Val Ala 355 360 365 Glu Ile Met Thr Arg Ile Asn Asp Gln Tyr Pro Gln Leu Asn Leu Thr 370 375 380 Lys Asp Leu Ser Gly Leu Leu Asp Leu Ala Ala Leu Asp Gln Asp Ser 385 390 395 400 Gly Gly Pro Lys Glu Asn Leu Phe Thr Val Ala Ser Arg Ile Pro Thr 405 410 415 Tyr Arg Cys Glu Phe Leu Asn Lys Gln Tyr Phe Val Leu Met His Thr 420 425 430 Asp Cys Ile Asp Ala Tyr Trp Lys Gln Asn Ile Ile Val Pro Glu Asp 435 440 445 Ala Gln Leu Gln Gly Leu Thr Asp Gln Asp Leu Thr Ser Arg Ile Phe 450 455 460 Tyr Cys Asp Leu Gly Leu Ser Leu Pro Thr Phe Lys Gln Gln Ile Met 465 470 475 480 Val Ser Arg His Glu Tyr Phe Asn Pro Arg Leu Pro Val Tyr Arg Trp 485 490 495 Val Leu Asp Phe Asp Leu Lys Val Thr Glu Gly Arg Arg Thr Leu Asn 500 505 510 Asp Ile Tyr Asn Ile Cys Val Thr Leu Arg Gln Val Ile Leu Glu Thr 515 520 525 Leu Gln Leu Ile Gly Pro Leu Lys Pro His His Pro Val Tyr Phe Phe 530 535 540 Lys Ser Ala Cys Pro Ala Val Thr Trp Pro Asp Asp Ile Ser Asp Thr 545 550 555 560 Ala Phe Cys His Cys Asp Thr Lys Ile Gly Met Arg Ile Val Thr Pro 565 570 575 Phe Pro Ile Gly Tyr Cys Leu Val Gly Ser Ala Pro Leu Val Ser Leu 580 585 590 Thr Asn Ile Leu Asn Arg Val Val Lys Leu Asp Thr Arg Leu Ala Ser 595 600 605 Glu Tyr Pro Gly Ile Leu Glu Asp Lys Gly Pro Phe Asp Ser Gly Ile 610 615 620 Tyr Ala Lys Gly Arg Cys Val Arg Val Pro His Cys Tyr Lys Val Gly 625 630 635 640 Pro Gly Gly Glu Leu Ser Arg Leu Leu Lys Ile Ile Ile Cys His Pro 645 650 655 Glu Glu Ser Asp Lys Ser Ala Tyr Leu Lys Asn Ala Phe Lys Val Ser 660 665 670 Asn Leu Leu His His Ala Pro Gly Asp Ser Val Thr Lys Asn Gly His 675 680 685 Leu Val Tyr Ala Ile Ala Asp Glu Asn Glu Gly Phe Leu Glu Ser Lys 690 695 700 Thr Lys Asn Asn Leu Pro Lys Thr Ile Thr Asp Leu Ala Glu Lys Ile 705 710 715 720 Glu Arg Thr Thr Glu Lys Pro Leu Ile Asp Trp Ala Ala Thr Ala Val 725 730 735 Trp Pro Lys Leu His Asp Thr Ile Gln Arg Phe Phe Pro Asp Asp Arg 740 745 750 Ile Gly Gln Phe Ala Ser Val Ser Phe Met His Ser Gly Asp Asn Ile 755 760 765 Ile Gln Val Arg Pro Gln Lys Gly Asn Asn Phe Phe Cys Ile Asn His 770 775 780 Lys His Arg Asn His Thr Gln Thr Val Arg Val Phe Leu Thr Leu His 785 790 795 800 Ser Thr Lys Glu Ser Glu Val Thr Val Thr Phe Met Ser Gln Cys Phe 805 810 815 Ala Ala Lys Cys Asn His Asn Ser Pro Thr Ala His Phe Ser Phe Met 820 825 830 Val Pro Ile Thr Cys Thr 835 96 91 PRT Japanese Macaque Herpesvirus 96 Met Leu Ser Pro Glu Cys Met Lys Leu Thr Asp Ala Asn Trp Pro Met 1 5 10 15 Arg Ser Ser Gly Lys Lys Arg Cys Met Val Ser Cys Ser Phe Gly His 20 25 30 Thr Ala Val Ala Ala Gln Ser Ile Ser Gly Phe Ser Val Val Arg Ser 35 40 45 Ile Phe Ser Ala Lys Ser Val Ile Val Phe Gly Arg Leu Phe Leu Val 50 55 60 Leu Leu Ser Arg Lys Pro Ser Phe Ser Ser Ala Ile Ala Tyr Thr Arg 65 70 75 80 Trp Pro Phe Leu Val Thr Glu Ser Pro Gly Ala 85 90 97 89 PRT Japanese Macaque Herpesvirus 97 Met Ala Gln Ala Met Val Ser Leu Glu Tyr Met Lys Asp Ile Leu Asp 1 5 10 15 Gly Lys Lys Thr Ser Tyr Gly Ser Tyr Asn Phe Tyr Leu Lys Pro Gln 20 25 30 Leu Thr Lys Arg Leu Val Leu Tyr Ala Leu His Ala Val Arg Val Ser 35 40 45 Arg Thr Asn Leu Phe Tyr Arg Gly His Ile Ile Ile Gly Leu Arg Arg 50 55 60 Leu Leu Ile Gly Arg Asp Gly Arg Pro Val Pro Asp Ala Gly Ala Arg 65 70 75 80 Thr Val His Gly Thr Ala Gln Leu Ser 85 98 440 PRT Japanese Macaque Herpesvirus 98 Met Arg Tyr Val Phe His Ala Leu Ile Cys Phe Ile Gly Gly Ile Ser 1 5 10 15 Ser Ser Asp Phe Asp Asp Ser Ser Ser Asp Glu Met Asp Asp Leu Ser 20 25 30 Pro Thr Pro Glu Pro Glu Pro Ser Thr Ala Pro His Ser Phe Pro Glu 35 40 45 Gly Pro Lys Ser Lys Val Val Ala Leu Pro Lys Ile Arg Lys Arg Ser 50 55 60 Arg Ser Lys Thr Pro Val Lys Ile Glu His Arg Ser Pro Leu Asn Arg 65 70 75 80 Ser Arg Ser Arg Ser Arg Thr Arg Ser Gly Ser Gly Gln Arg Thr Ser 85 90 95 Ser Thr Tyr Val Lys Arg Phe Lys Pro Thr Val Asp Ala Pro Arg Ser 100 105 110 Arg Glu Pro Trp His Arg Gly Gly Lys Gly Lys Ala Pro Phe Ile Arg 115 120 125 Arg Asn Ala Leu Ala Glu Arg Gly Arg Arg Thr Tyr Gly Asn Glu His 130 135 140 Arg Gly Lys Ser Ala Leu Thr Arg Asn Ile Lys Glu Ser Ile Lys Lys 145 150 155 160 Met His Leu Pro Ser Thr Met Leu Ser Arg Pro His Asp Lys Lys Val 165 170 175 Phe Glu Gly Leu Leu Pro Arg His Leu Glu Gln Cys Phe Gln Val Cys 180 185 190 Leu Pro Ala Pro Pro Pro Leu Arg Pro Glu Val Phe Thr Asp Arg Gln 195 200 205 Leu Thr Ala Ile Val Lys Ser Gly Gly Arg Arg Asp Ala Leu Val Ala 210 215 220 Lys Lys Val Ser Leu Ala Lys Val Met Ser Met Tyr Lys Pro Leu Leu 225 230 235 240 Thr Phe Val Thr Gly Arg Asn Asn Gln Ala His Trp Leu Ala Thr Arg 245 250 255 Lys Asn Thr Leu Ala Ser Ala Gly Leu Glu Ala Leu Ala Ala Phe Ile 260 265 270 Glu Glu Gly Leu Ala Trp Ala Gln Val Cys Val Ser Gln Asn Arg Ser 275 280 285 Leu Asn Asp Ser Asn Leu Asp Ile Ile Leu Asp Ser Ser Gln Ser Val 290 295 300 Cys Thr Trp Phe Ile Ser Lys Ile Arg His Leu His Ile Gln Cys Phe 305 310 315 320 Leu Glu Asn Gln Gly Glu Ile Ser Leu Val Lys Gln Leu Thr Tyr Leu 325 330 335 Val Cys Ile Asn Asn Arg Leu Ala Glu Ala Ala Asn Leu Ala Gly Glu 340 345 350 Val Lys Leu Asn Phe Lys Phe Ala Met Leu Ile Gly Phe Ala Leu Thr 355 360 365 Leu Pro Ala Leu Leu Ala Glu Gln Lys Leu Ser Gly Glu Ser Leu Tyr 370 375 380 Leu Phe Arg Ser Phe Leu Glu Lys Tyr Arg Pro Gly Asp Val Met Gly 385 390 395 400 Leu Leu Asn Ser Ile Val Val Glu His Tyr Thr Lys Cys Arg Ser Ala 405 410 415 Glu Cys Val Ile Thr Thr Arg Ala Met Val Gly Ser Gly Glu Asn Asn 420 425 430 Lys Gly Leu Phe Phe Phe Pro Ala 435 440 99 413 PRT Japanese Macaque Herpesvirus 99 Met Ala Thr Trp Cys Pro Pro His Ser Gly Gly Pro Ser Ala Met Gly 1 5 10 15 Leu Arg Glu Trp Ile Val Thr His Ala Asn Leu Gly Thr Tyr Ser Gly 20 25 30 Leu Phe Trp Ala Asp Asp Glu Lys Thr Arg Val Val Leu Ala Thr Thr 35 40 45 Thr Ala Trp Thr Val Glu Phe Asp Tyr Pro Arg Asp Gly Lys Val Tyr 50 55 60 Glu Asp Tyr Cys Asn Gln Arg Asn Ile Pro Leu Pro Ser Gly Arg Pro 65 70 75 80 Arg Leu Cys Gln Ala Lys Ala Arg Leu Leu Gly Ala Ile Arg Lys Ser 85 90 95 Ala Tyr Phe Val Glu Glu Lys Asn Phe Leu Arg Arg Ser Phe Ser Phe 100 105 110 Pro Thr Val Val Phe Arg Leu Arg Ser Asn Glu Glu Met Ser Cys Arg 115 120 125 Leu Cys Pro Arg Ala Ser Gly Val Ala Ala Glu Leu Arg Gly Leu Arg 130 135 140 Phe Arg Met Phe Lys Arg Lys Gly Ala Asp Asp Val Gly Arg Val Thr 145 150 155 160 Glu Tyr Thr Val Lys Gln Leu Leu Gly Leu Leu Arg Thr Arg His Ala 165 170 175 Gly Ala Ser Thr Met Thr Ala Pro Ala Thr Glu Ala Ser Ala Thr Thr 180 185 190 Ala Gly Glu Asp Gly Arg Gln Asp Glu Ser Glu Gly Gly Ala Val Ala 195 200 205 Leu Pro Glu Glu His Thr Pro Pro Leu Ser Val Ser Ser Gly Leu Ser 210 215 220 Ala Cys Leu Ala Pro Ser Val Asp Asp Pro Trp Gly Phe Met His Ile 225 230 235 240 Gln Val Tyr Tyr Tyr Gly Phe Leu Gln Ser Gln Val Phe Thr Arg Thr 245 250 255 Gly Met Gly Val Arg Leu Ser Thr Arg Pro Thr Asp Lys Asn Glu His 260 265 270 His Val Cys Met Ala His Gly Pro Leu Gln Leu Trp Leu Pro Pro Ala 275 280 285 Pro His Met Asp Asp Asp Val Met Leu Ser Arg Leu Val Asn Ala Leu 290 295 300 Asn Ala Leu Glu Asp Gly Ile Val Leu Ser Ser Cys Gln Tyr Gly Ile 305 310 315 320 Met Met Asn Gly Tyr Gly Phe Leu Asn Leu Trp Phe Arg Gly Asn Thr 325 330 335 Leu Asn Thr Leu Glu Pro Thr Arg Val Pro Ser Gly Val Gly His Arg 340 345 350 Ile Phe Asp Thr Asp Asp Tyr Ile Thr Lys Leu Ala Gln Ser Pro Arg 355 360 365 Pro Ser Asp Pro Gly Pro Pro Asp Pro Phe Ala Gln Ile Trp Val Ala 370 375 380 Ala Trp Ser Leu Tyr Glu Glu Glu Asp Leu Ser Gln Ala Pro Ile Cys 385 390 395 400 Ile Ile Val His Gln Arg Glu Ile Tyr Arg His Phe Glu 405 410 100 81 PRT Japanese Macaque Herpesvirus 100 Met Ala Pro Asn Thr Gln Lys Asp Arg Leu Ile Gln Ile Ala Ala Glu 1 5 10 15 Cys Val Pro Arg Val Thr Gln Pro Arg Pro Leu His Ser Arg Pro Ala 20 25 30 Tyr Arg Leu His Arg Arg Trp Leu Arg Thr Pro Arg Trp Pro Gly Arg 35 40 45 Ser Trp Trp Arg His Arg Arg Asp Gly Tyr Glu Ala Ala Arg Ala Ala 50 55 60 Ala Leu Pro Cys Ile Gln Leu Pro Cys Pro His Arg Arg Arg Pro Cys 65 70 75 80 Ala 101 138 PRT Japanese Macaque Herpesvirus 101 Met Arg Leu Pro Val Gly Ala Asp Val Cys Ser Arg His Glu Ile Ile 1 5 10 15 Pro Pro Ala Ala Thr Asn Ser Leu Ser Ala Gln Ser Ala Gly Tyr Arg 20 25 30 Leu Ile Ser Leu Thr Ser Thr Pro Pro His His Leu His Arg Ser Cys 35 40 45 Pro Cys Pro Asp Cys Pro Leu Asn Leu Val Arg Ser Arg Pro Ala Leu 50 55 60 Leu Pro Gly Gln Ala Ile Asp Ser Ser Pro Leu Arg Asp Leu Pro Tyr 65 70 75 80 Gly Arg Asn Arg Arg His Glu Pro Leu Met Phe Gln Leu Ser Arg Gly 85 90 95 Lys Asn Asn Pro Arg Cys Arg Thr Gln Thr Arg Phe Arg Thr Arg Asn 100 105 110 Ala Val Leu Trp Arg Trp Val His Gly Arg Asp Ser Ala Thr Glu Pro 115 120 125 Thr Asp Thr Gly Arg Phe Val His Asn Leu 130 135 102 413 PRT Japanese Macaque Herpesvirus 102 Met Ala Gly Arg Gly Val Asp Ile Lys Ala Trp Leu Val Ala Ala Val 1 5 10 15 Glu Ser Ser Glu Tyr His Gly Leu Val Trp Glu Asn Glu Asp Lys Thr 20 25 30 Val Val Arg Val Pro Trp Asn Lys Val Thr Ala Ala Arg Ser Asp Ser 35 40 45 Glu Lys Phe Phe Asp Asp Tyr Cys Asn Met Arg Gly Ile Cys Gln Gly 50 55 60 Glu Lys Pro Pro His Tyr Gly Arg Phe Arg Lys Met Arg Phe Leu Tyr 65 70 75 80 Asp Met Arg His His Lys Ser Ile Arg Glu Leu Lys Phe Ile Asn Lys 85 90 95 Ala Tyr Gly Arg Ser Glu Ala Arg Tyr Arg Leu Phe Arg Leu Leu Pro 100 105 110 Glu Pro Val Val Ser Cys Ala Met Cys Asn Leu Met Ser Ser Thr Glu 115 120 125 Thr Gln Cys Leu Gly Leu Thr Ser Glu Phe Arg Tyr Asp Gln Trp Gly 130 135 140 Gly Phe Gly Arg Glu Arg Arg Arg Val Phe Thr Ala Thr Val Leu Ala 145 150 155 160 Arg Ser Trp Met Asp Lys Asn Lys Arg Val Arg Glu His Arg Leu Pro 165 170 175 Gly Ala Ile Gln Leu Thr Phe Leu Tyr Phe Gly Ser Thr Val Gly Leu 180 185 190 Glu Arg Val His Ala Gly Thr Arg Val Cys Ser Arg Pro Tyr Pro Val 195 200 205 Leu Ala Gly His Ala Cys Cys Phe Gln Asp Glu Arg Thr Leu Phe Leu 210 215 220 Pro Pro Pro Gly Val Val Asp Cys Ser Phe Ala Arg Glu Asp Leu Arg 225 230 235 240 Gly Met His Lys Lys Cys Glu Lys Gly Leu Leu Ile Ala Leu Thr Asp 245 250 255 Thr Gly Ile Ser Val Lys Asn Leu Glu Asn Arg Glu Met Lys Val Leu 260 265 270 Thr Asn Asn Glu Glu Glu Tyr Lys Asp Leu Pro Ser Arg Gln Pro Val 275 280 285 Gln Val Phe Asp Met Val Asp Tyr Leu Arg Ala Leu Ala Arg Ser Pro 290 295 300 Lys Pro Gly Asp Asp Pro Pro Arg Asp Tyr Ala Gln Ile Ala Leu Cys 305 310 315 320 Leu Ser Val Gln Ser Pro Asn Pro Ala His Ala Pro Ile Ala Ile Arg 325 330 335 Leu Arg Tyr Val Cys Glu Thr Ser Ser Val Cys Gly Thr Glu Gly Cys 340 345 350 Phe Tyr Pro Gly Thr Ile Gly Thr Ser Glu Ala Arg Val Ala Gly Ser 355 360 365 Phe His Met Glu Asp Pro Gly Glu Gly Thr Ser Gln Ser Leu Asp Pro 370 375 380 Ala Val Glu Leu Gly Asp Ser Gly Pro Asp Ser Met Asp Asn Pro Asp 385 390 395 400 Thr Gly Thr Ser Gly Glu Asp Asp Gly Val Ala Cys Ser 405 410 103 91 PRT Japanese Macaque Herpesvirus 103 Met Gly Gly Ile Arg Arg Leu Asn Arg Gln Thr Gln Gly Asp Leu Cys 1 5 10 15 Ile Ile Ser Arg Trp Val Val Ser Arg Leu Arg Gly Pro Cys Lys Ser 20 25 30 Ser Lys Ile Ile His His Ile Lys His Leu Asn Gly Leu Pro Gly Arg 35 40 45 Gln Val Leu Ile Leu Leu Leu Ile Val Ser Lys His Phe His Phe Pro 50 55 60 Val Leu Gln Val Leu Tyr Gly Asn Ala Ser Ile Arg Lys Gly Asn Gln 65 70 75 80 Gln Thr Leu Leu Ala Leu Phe Val His Ala Pro 85 90 104 351 PRT Japanese Macaque Herpesvirus 104 Met Glu Arg Pro Val Arg Val Thr Lys Pro Ser Ser Leu Arg Gly Trp 1 5 10 15 Leu Val Glu Cys Cys Glu Thr Gly Arg His Pro Gly Met Arg Trp Ile 20 25 30 Asp Asp Glu Arg Thr Leu Ile Arg Ile Pro Trp Asn His Asp Arg Gly 35 40 45 Ser Arg Gly Val Glu Glu Ser Glu Lys Asn Ile Phe Ile Asp Tyr Cys 50 55 60 Arg Ser Arg Gly Ile Leu His Ala Ala Gly Arg Glu Leu Thr Ala Lys 65 70 75 80 Glu Cys Lys Asn Trp Leu Ser Ser Ala Ile Arg His Ser Gln Thr Val 85 90 95 Ser Asp Val Ser Thr Asn Asp Asp Leu Ser Thr Pro Tyr Pro Asn Arg 100 105 110 Cys Arg Thr Ile Arg Leu Leu Pro Ile Thr Val Arg Ser Cys Ala Arg 115 120 125 Cys Asp Gln Ala Ser Gly Thr Thr Ala Met Leu Arg Gly Leu Arg Glu 130 135 140 Glu Ala Val Asn Lys Phe Gly Pro Val Gly Ala Gly Val Gln Tyr Thr 145 150 155 160 Gly Ala Val Gly Ala Gly Gly Glu Gln Cys Trp Met Leu Arg Ile Thr 165 170 175 Phe Tyr Tyr Tyr Gly Asp Arg Phe Gly Glu Val Val Thr Glu Ser Pro 180 185 190 Asn Gly Ile Arg Val Leu Pro Leu Ser Glu Arg Arg Ala Gln Gly His 195 200 205 Ile Cys Val Ala Pro Ile Ala Glu Gln Ala Leu Val Pro Glu Ile Pro 210 215 220 Ser His Leu Val Glu Phe Gln Ala Glu Ala Leu Arg Phe Leu Asp Lys 225 230 235 240 Asp Leu Leu Arg Gly Leu Ala Phe Trp Ala Asp Pro Ser Gly Ile Tyr 245 250 255 Ile Arg Trp Leu Gly His Ser Met Ala Phe Val Gln Gly Asn Val Glu 260 265 270 Ser Pro Gly Ala Ile Val Val Leu Ser Cys Ala Asn Ala Cys Arg Ala 275 280 285 Phe Asn Leu Val Asp Tyr Met Lys Gly Met Ala Arg Thr Pro Arg Asp 290 295 300 Gly Thr Ala Pro Pro Gln Ala Cys Val Tyr Leu Tyr Phe Gly Gly Val 305 310 315 320 Pro Thr Pro Glu Gly Gly Val Gln Ser Thr Val Pro Leu Ile Ile Gln 325 330 335 Leu Trp His Glu Cys Leu Trp Gln Ala Leu Ser Ala Ala Asn Val 340 345 350 105 361 PRT Japanese Macaque Herpesvirus 105 Met Ala Ile Arg Asp Ser Asn Tyr Ser His Leu Arg Ser Trp Thr Leu 1 5 10 15 Tyr His Leu Asn Glu Lys Thr Tyr Ser Asp Leu Thr Trp Cys Asp Gln 20 25 30 Glu Lys Lys Thr Phe Lys Leu Ser Trp Lys Lys Gly Ala Ala Gly Thr 35 40 45 Pro Ala Val Val Ala Tyr Cys Ala Gln Arg Gly Leu Gln Val Gly Ile 50 55 60 Asp Gly Asn Val Phe Glu Cys Lys Arg Arg Phe Leu Arg Gly Leu Arg 65 70 75 80 Glu Asn Ala Gly Phe Gln Glu Cys Glu His Gly Val Val Arg Thr His 85 90 95 Gly Gly Gly Trp Thr Ala Phe Arg Val Lys Pro Leu Met Asp Ser Gly 100 105 110 Cys Phe Ala Cys Ile Leu Asp Glu Asn Ser Glu Gly Ile Ile Asn Tyr 115 120 125 Leu Glu Gln Val Cys Gly Ile Gly Leu Glu Pro Gly Met Pro Leu Pro 130 135 140 Ala Pro Leu Pro Thr Leu Val Pro Pro Thr Arg Ser Ala Tyr Ala Arg 145 150 155 160 Ala His Arg Leu Gly Val Pro Glu Ala Pro Leu Pro His Gln Ile Val 165 170 175 Pro Phe Trp Arg Leu Arg Ile Gln Val Phe Tyr Phe Gly Val Leu Ala 180 185 190 Leu Asp His Thr Ser Gln Asp Arg Arg Gly Val Arg Leu His Pro Arg 195 200 205 Pro Val Pro Arg Pro Gly His Leu Cys Phe Tyr Gly Thr Gly Phe Thr 210 215 220 Val Trp Phe Pro Ser Pro Asp Pro Gly Lys Leu Thr Pro Asp Gln Ile 225 230 235 240 Thr Gln Ile Asn Thr Met Leu Val Thr Tyr Asn Glu Gly Ile Tyr Val 245 250 255 His Gly Asn Glu Thr Gly Val Tyr Val Asp Asn Arg Asn Arg Glu Thr 260 265 270 Leu Tyr Ala Ala Gly Asn Asp Cys Asn Gly Asp Ile Ile Gln Arg Glu 275 280 285 Val Met Phe Leu Ser Lys Gln Gln Ile Phe Tyr Phe Met Gly Phe Met 290 295 300 Arg Lys Leu Ala Arg Ser Pro Val Pro Glu Ser His Ala Pro Cys Asn 305 310 315 320 Gly Ala Thr Leu Tyr Leu Ser Gln Gln Pro Gly Ala Gln Glu Ser Pro 325 330 335 Gln Val Pro Ile Ser Val Val Val Cys Gln Asp Glu Leu Val Gln Gly 340 345 350 Gln Met Asn Pro Ser Arg Trp Cys Ala 355 360 106 135 PRT Japanese Macaque Herpesvirus 106 Met Ala Leu Trp Tyr Arg Gly Ala Gly Lys Leu Ser His Glu Thr His 1 5 10 15 Glu Ile Lys Asn Leu Leu Phe Arg Glu Glu His Asp Leu Ser Leu Asn 20 25 30 Asn Ile Thr Ile Thr Val Val Thr Arg Ser Val Lys Arg Phe Pro Val 35 40 45 Pro Ile Ile Asp Val His Ser Gly Phe Ile Ala Val Tyr Val Asp Ala 50 55 60 Leu Val Ile Arg Asp Gln His Cys Val Tyr Leu Arg Tyr Leu Ile Trp 65 70 75 80 Ser Gln Phe Ser Arg Ile Trp Arg Trp Lys Pro Asn Gly Lys Pro Gly 85 90 95 Ala Val Lys Thr Gln Met Thr Gly Thr Trp Asn Arg Ala Arg Met Gln 100 105 110 Thr Asn Thr Ser Ser Ile Leu Gly Arg Met Ile Gln Cys Gln Asn Ala 115 120 125 Lys Ile Lys His Leu Asn Ser 130 135 107 385 PRT Japanese Macaque Herpesvirus 107 Met Ala Ala Gly Glu Ser Arg Arg Gly Pro Ser Arg Tyr Gly Met Ala 1 5 10 15 Leu Arg Glu Trp Leu Ile Ser Lys Ala Asp Ser Gly Phe Tyr Pro Gly 20 25 30 Leu Phe Trp Ala Asp Glu His Lys Thr Arg Leu Val Leu Ala Ala Thr 35 40 45 Ser Pro Ser Leu Pro Asn Tyr Asp Tyr Gln Arg Asp Gly Gln His Tyr 50 55 60 Asp Ala Tyr Cys Asp Leu Arg His Ile Pro Leu Pro Ser Gly Arg Gly 65 70 75 80 Arg Leu Cys Gln Ala Lys Gly Arg Leu Leu Gly Ala Ile Arg Lys Ser 85 90 95 Lys Tyr Phe Asp Glu Asp Lys Asp Phe Pro Thr Asp Gln Phe Pro Phe 100 105 110 Thr Ala Val Val Phe Arg Leu Arg Ser Phe Glu Glu Met Ser Cys Pro 115 120 125 Val Cys Pro Arg Val Asp Ala Leu Arg Leu Glu Leu Arg Asn Met Arg 130 135 140 Phe Ala Met Leu Gly Arg Gly Met Leu His Ala Phe Pro Glu Ser Ser 145 150 155 160 Val Gly Asp His Glu Ala Arg His Leu Glu Gly Gln Glu Gly Gly Asp 165 170 175 Asp Ala Arg Asp Asp Asp Ala Pro Tyr Ser Ser Gly Val Leu Arg Ala 180 185 190 Arg Leu Met Ala Cys Ala Ala Pro Ser Ala Gly Asp Pro Trp Gly His 195 200 205 Met His Ile Lys Ile Tyr Tyr Tyr Gly Gln Leu Gln Ala Glu Leu Ser 210 215 220 Thr Ala Thr Gly Gln Gly Ile Arg Leu Ser Ser Arg Pro Thr Asn Lys 225 230 235 240 Ser Gly His His Val Cys Val Leu Asp Gly Pro Leu Gln Ala Trp Phe 245 250 255 Pro Pro Ile Pro Gln Ile Thr Asp Thr Ser Met Gly Gln Arg Leu Glu 260 265 270 Asp Ala Leu Lys Trp Leu Val Asp Gly Ile Ile Phe Cys Ser Thr Ser 275 280 285 Arg Gly Ile Val Phe Thr Ile Thr Gly Ala Pro Asn Val Trp Phe Gln 290 295 300 Gly Asn Thr Val Glu Pro Arg Asn Phe Pro His Arg Ala Tyr Thr Gly 305 310 315 320 Met His Val Trp Ala Phe Asp Thr Asp Arg Tyr Leu Leu Asp Ile Ala 325 330 335 Arg Ser Pro Ser Pro His Asp Thr Asp Pro Pro Ala Ala Phe Val Lys 340 345 350 Leu Trp Val Ser Gly Cys Ser Leu Gly Glu Glu Arg Asn Val Ser Arg 355 360 365 Ala Pro Leu Ser Met Thr Val His Gln Thr Glu Ile Tyr Arg His Phe 370 375 380 Glu 385 108 81 PRT Japanese Macaque Herpesvirus 108 Met Thr Gln Leu Arg Pro Tyr Cys Asp Lys His Arg Glu Ser Gly Thr 1 5 10 15 Arg Val Leu Leu Trp Pro Phe Cys Gln Met Asn Pro Thr Gly Asn Ile 20 25 30 Tyr Phe Leu Gln Tyr Gly Ala Lys Val Glu Thr Glu Val Leu Pro Val 35 40 45 Val Pro Glu Ala Pro Pro Arg Thr Pro Asp Gly Pro Ser Ser Pro Leu 50 55 60 Leu Leu Pro Val Ala Leu Ser Pro Val Ser Thr Asp Thr Ser Ser His 65 70 75 80 Thr 109 390 PRT Japanese Macaque Herpesvirus 109 Met Ala Glu Gln Asn Met Asp Leu Lys Ala Trp Phe Ile Asp Ala Val 1 5 10 15 Glu Ser Arg Arg Tyr Pro Gly Val Val Trp Asp Asp Asp Asp Arg Thr 20 25 30 Ile Ile Arg Ile Pro Trp Asn Arg Ser Thr Asp Ser Arg Ile Asp Glu 35 40 45 Glu Tyr Asn Lys Ile Phe Asp Asp Phe Cys Leu Ala Arg Gly Val Cys 50 55 60 Gln Ser Gly Ser Thr Ala His Ala Asn Lys Phe Lys Lys Ile Arg Met 65 70 75 80 Leu Tyr Ala Val Arg Ser His Arg Tyr Leu Arg Glu Leu Thr Pro Pro 85 90 95 Ser Lys Ala Gly Gly Val Ser Gly Glu Arg Tyr Arg Leu Phe Gln Leu 100 105 110 Leu Pro Glu Val Thr Asn Gly Cys Asp Leu Cys Asn Leu Ile Ala Thr 115 120 125 Thr Ser Leu His Ser Cys Ser Met Gly Ser Gly Val Arg Asp Asp Phe 130 135 140 Phe Glu Gln Ala Arg Arg Pro Arg Ala Arg Leu Pro Leu Arg Val Ser 145 150 155 160 Ile Gln Arg Arg Lys Ala Arg Leu Gln Gly Ser Pro Ala Gln Ala Ala 165 170 175 Pro Gly Ala Ile Glu Val Ser Phe Phe Tyr Phe Gly Glu Asn Val Gly 180 185 190 Val Glu Ile Leu Arg Ser Gly Cys Gly Val Arg Ile Cys Gly Leu Pro 195 200 205 Asp Pro Lys Arg Pro Gly His Leu Cys Cys Ala Asp Asn Pro Leu Thr 210 215 220 Arg Phe Leu Pro Ser Ala Gln Leu Val Pro Cys Glu Phe Ala Arg Ala 225 230 235 240 Asp Leu Gln Ala Leu Gln Lys Thr Cys Glu Arg Gly Leu Ile Cys Val 245 250 255 Met Val Glu Ser Gly Ile Cys Val Lys Asn Leu Glu Glu Arg Asn Met 260 265 270 Thr Ala Leu Thr Asn Tyr Ser Glu Asn Tyr Tyr Glu Leu Gln Pro Thr 275 280 285 Gln Gln Phe Gln Val Phe Asp Leu Leu His Tyr Leu Arg Ala Leu Ala 290 295 300 Arg Ser Pro Thr Pro Gly Asp Leu Pro Pro Arg Asp Cys Ala Trp Ile 305 310 315 320 Phe Leu Cys Pro Ser Thr Gln Ser Glu Asn Thr Trp Asp Ala Pro Ile 325 330 335 Ala Leu Lys Leu Arg Tyr Val Cys Asp Asp Val Ser Val Glu Thr Gly 340 345 350 Asp Ser Ala Thr Gly Ser Asn Ser Gly Asp Glu Gly Pro Ser Gly Val 355 360 365 Arg Gly Gly Ala Ser Gly Thr Thr Gly Ser Thr Ser Val Ser Thr Phe 370 375 380 Ala Pro Tyr Trp Arg Lys 385 390 110 86 PRT Japanese Macaque Herpesvirus 110 Met Leu Arg Ser Ser Arg Phe Phe Thr Gln Ile Pro Asp Ser Thr Ile 1 5 10 15 Thr Gln Ile Arg Pro Leu Ser His Val Phe Cys Arg Ala Cys Lys Ser 20 25 30 Ala Leu Ala Asn Ser His Gly Thr Asn Cys Ala Asp Gly Arg Lys Arg 35 40 45 Val Asn Gly Leu Ser Ala Gln His Arg Cys Pro Gly Arg Leu Gly Ser 50 55 60 Gly Arg Pro His Ile Arg Thr Pro Gln Pro Glu Arg Lys Ile Ser Thr 65 70 75 80 Pro Thr Phe Ser Pro Lys 85 111 91 PRT Japanese Macaque Herpesvirus 111 Met Arg Leu Ser Val Asp Leu Phe His Gly Ile Arg Ile Met Val Leu 1 5 10 15 Ser Ser Ser Ser His Thr Thr Pro Gly Tyr Arg Arg Asp Ser Thr Ala 20 25 30 Ser Met Asn Gln Ala Phe Lys Ser Met Phe Cys Ser Ala Ile Ser Arg 35 40 45 Val His His Leu Tyr Arg Ala Gly Gln Leu Lys Tyr Arg Ala His Arg 50 55 60 Thr Thr Ser Leu Arg Asp Gln Lys Asn Leu Asp Leu Lys Glu Ala Tyr 65 70 75 80 Leu Tyr Thr Pro Thr Gly Gln Leu Ser Asn Lys 85 90 112 355 PRT Japanese Macaque Herpesvirus 112 Met Ala Glu Gly Arg Ala Gly Ser Ile Arg Val Asn Arg Pro Ser Gly 1 5 10 15 Leu Arg Ala Trp Leu Leu Asp Cys Cys Asp Asn Gly Lys His Pro Gly 20 25 30 Met His Trp Leu Asn Glu Glu Lys Thr Leu Val Arg Leu Pro Trp Asn 35 40 45 His Leu Lys Gly Ala Gly Gly Val Ser Glu Asn Glu Lys Asn Ile Phe 50 55 60 Leu Asp Tyr Cys Gln Phe Lys Gly Ile Arg His Thr Gly Asn Arg Pro 65 70 75 80 Leu Ser Leu Arg Glu Cys Lys Asn Trp Leu Ala Ser Ala Ile Arg His 85 90 95 Ser Gln Thr Val Glu Asp Val Ser Thr Glu Glu Asn Leu Ser Ala Pro 100 105 110 Ala Pro Tyr Arg Cys Arg Val Ile Arg Leu Leu Pro Ile Phe Val Arg 115 120 125 Ser Cys Pro Leu Cys Asn Glu Ala Asp Ala Thr Gly Gly Met Leu Leu 130 135 140 Asp Leu Arg Asn Glu Val Thr Ala Arg Phe Leu Tyr Leu Gly Ala Gly 145 150 155 160 Arg Glu Tyr Glu Gly Ala Val Gly Ser Asp Gly Val Arg Cys Trp Met 165 170 175 Ile Arg Leu Val Ile Tyr Tyr Tyr Gly Arg Leu Val Gly Asn Met Glu 180 185 190 Val Gly Ser Pro Asn Gly Val Arg Leu Leu Pro Ala Pro Lys Gln Pro 195 200 205 Leu Gln Gly His Val Cys Ala Gly Ile Lys Pro Glu Gln Val Met Leu 210 215 220 Pro His Asn Pro His Asn Leu Leu Pro Tyr Gln Thr Ser Met Leu Arg 225 230 235 240 Trp Leu Ala Lys Glu Ile Ile Arg Gly Leu Met Ile Tyr Ala Asp Gly 245 250 255 Ser Gly Ile Tyr Val Arg Tyr Met Gly His Val Pro Ala Phe Leu Leu 260 265 270 Gly Asn Gly Gly Ser Pro Glu Pro Val Asp Met Ile Asn Ser Gly Arg 275 280 285 Val Ala Arg Val Phe Ser Leu Val Gln Tyr Leu Ser Ala Val Ser Ala 290 295 300 Thr Pro Pro His Gly Thr Leu Phe Pro Ala Ala Tyr Ala Ser Leu His 305 310 315 320 Ile Gly Gly Val Pro Thr Pro Glu Gly Glu Pro Cys Pro Thr Ile Pro 325 330 335 Leu Ser Ile Gln Met Trp His Glu Cys Leu Trp Arg Ala Cys Gly Asp 340 345 350 Ala Ala Met 355 113 364 PRT Japanese Macaque Herpesvirus 113 Met Ala Glu Ser Glu Ile Thr His Asn His Leu Arg Arg Trp Ile Ile 1 5 10 15 Ser Asn Leu Glu Ala Asn Thr Tyr Pro Asp His Leu Arg Trp Cys Asp 20 25 30 Glu Glu Lys Arg Ser Phe Lys Leu Ser Trp His Arg Gly Met Gln Gly 35 40 45 Met Gln Pro Val Val Ala Tyr Cys Leu Asp Arg Asp Leu Gln Cys Gly 50 55 60 Arg Gln His Asn Val Ser Asp Cys Arg Lys Arg Leu Leu Arg Val Leu 65 70 75 80 Arg Glu Asn Ala Gly Phe Glu Gln Asp Asp Thr Arg Ala Thr Thr Thr 85 90 95 Asn Ser Gly Gly Glu Arg Phe Phe Tyr Leu Lys Pro Ala Val Asp Pro 100 105 110 Leu Cys Tyr Ala Cys Ile Leu Asp Ser His Ser Glu Thr Val Ile Asn 115 120 125 Tyr Leu Glu Ala Ala Cys Val His Gly Leu Glu Pro Trp Thr Pro Leu 130 135 140 Pro Pro Gln Ala Pro Ala Glu Ala Ser Gly Ala Ala Arg Ser Val Tyr 145 150 155 160 Ala Arg Ala Ala Arg Leu Ala Ile Ala Ala Pro Pro His Pro Glu Gln 165 170 175 Ile Thr Pro Phe Trp Arg Leu Arg Ile Gln Val Phe Tyr Phe Gly Ser 180 185 190 Leu Val Ala Glu His Thr Gly Val Asp Arg Arg Gly Val Arg Leu His 195 200 205 Lys Arg Gln Asp Pro Lys Ala Gly His Ala Cys Tyr Tyr Gly Thr Ala 210 215 220 Phe Lys Met Trp Leu Pro Thr Pro His Glu Asn Gly Pro Leu Thr Pro 225 230 235 240 Glu Gln Arg Glu Thr Val Cys Glu Ile Ile Asn Tyr Cys Glu Glu Gly 245 250 255 Ile Phe Leu His Gly Asn Glu Leu Gly Ile Tyr Val Asp Asn Arg Thr 260 265 270 Arg His Thr Leu Ser Cys Ala Gly Asn Asp Ala Glu Gly Asn His Ala 275 280 285 Gln Arg Phe Val Arg Ser Cys Ala Lys Phe Gln Ile Phe Tyr Val Met 290 295 300 Gly Leu Leu Arg Lys Leu Ala Leu Ser Pro Val Pro Gly Asp Pro Val 305 310 315 320 Pro Ile Asn Ala Val Thr Leu Tyr Leu Gly Gly Arg Pro Gly Ser Arg 325 330 335 Lys Arg Pro Gln Val Pro Val Ile Leu Val Ile Cys Gln Asp Glu Leu 340 345 350 Thr His Gly Asp Ile Arg Pro Ala Arg Trp Ile Leu 355 360 114 86 PRT Japanese Macaque Herpesvirus 114 Met Ala Met Ser Trp Gly Tyr Met Trp Ile Thr Glu Gln Gly Thr Leu 1 5 10 15 Phe Pro Ala Pro Gly Thr Thr Gln Arg Glu Thr Thr His Ser Val Leu 20 25 30 Cys Asp Pro Val Pro Asn Phe Arg Phe Phe Met Leu Trp Val Tyr Cys 35 40 45 Ala Asn Ser Pro Phe Pro Pro Phe Pro Ala Thr Arg Phe Pro Ser Thr 50 55 60 Gln Ser Leu Phe Thr Leu Gly Val Ala Leu Ala Pro Val Lys Asp Pro 65 70 75 80 Arg Ser Leu Ser Phe Trp 85 115 102 PRT Japanese Macaque Herpesvirus 115 Met Asp Leu Ser Leu Gly Arg Pro Tyr Arg Leu Lys Leu Arg Arg Arg 1 5 10 15 Leu Val Val Arg Arg Gly Pro Phe Met Pro Glu Pro Pro Gly Trp Gln 20 25 30 Leu Pro Arg His His Thr Arg Ser Arg Ser Leu His Phe Gly Gly Tyr 35 40 45 Val Tyr Lys Phe Phe Ile Leu Asp Arg Trp Trp Arg Asn Thr Arg Ala 50 55 60 Trp Ile Val Glu Gly Tyr Ala Cys Ile Ser Ala Lys Thr Gln Lys Leu 65 70 75 80 Ala Met Arg Val Ile Met Gly Gln Arg Leu Arg Cys Gly Phe Gln Arg 85 90 95 Arg Met Arg Met Asp His 100 116 360 PRT Japanese Macaque Herpesvirus 116 Met Gly Thr Tyr Thr Ser Glu Ala Ser Leu Ala Trp Leu Ser Phe Met 1 5 10 15 Ser Gly Thr Val Ala Ala Ser Pro Phe Ile Leu Cys Phe Ile Tyr His 20 25 30 Ser Leu Tyr Phe Leu Glu Pro Leu Asn Ser Val Glu Asn Ile Ile Phe 35 40 45 Ser Trp Gly Ala Val Gly Leu His Gly Leu Leu Leu Leu Val Cys Val 50 55 60 Val Gly Pro Pro Ala Trp Leu Ser Arg Gln Val Asp Val Pro Cys Thr 65 70 75 80 Ile Ser Ala Ile Leu Ile Thr Ala Gly Ser Met Ala Ser Thr Leu Gly 85 90 95 Val Asp Leu Pro Trp Val Tyr Val Ser Phe Phe Val Gly Ser Cys Leu 100 105 110 Cys Leu Leu Leu Cys Val Val Val Ala Asn Asp Val Val Tyr Leu Cys 115 120 125 Pro Thr Ile Ala His Arg Tyr Tyr Glu Leu Gly Phe Phe Ala Ala Phe 130 135 140 Ser Val Tyr Tyr Phe Leu Val Leu Lys Asn Leu Phe Leu Ala Pro Val 145 150 155 160 Phe Leu Leu Pro Leu Val Ala Phe Ile Val Gly Gly Val Cys Ser Leu 165 170 175 Arg Ala Leu Arg Ser His Pro Leu Tyr Glu Ala Gly Leu Gln Arg Arg 180 185 190 His Ala Ile Phe Ser Leu Thr Ser Arg Arg Tyr Ile Thr Tyr Ser Ile 195 200 205 Lys Gln Ala Leu Glu Val Cys Gly Trp Asp Phe Tyr Leu Val Thr Val 210 215 220 Leu Ile Gly Gly Ala Ala Ala Gly Thr Leu Ser Val Gly Leu Thr Thr 225 230 235 240 Pro Leu Leu Leu Gly Leu Val His Tyr Phe Phe Val Phe His Val Gly 245 250 255 Leu Phe Cys Cys Ile Gly Leu Val Phe Arg Ser Asn Val Leu Ala Leu 260 265 270 Val Tyr Val Leu Ala Ala Ala Val Leu Leu Thr Leu Thr His Val Leu 275 280 285 Gly Pro Gly Thr His Asn Leu Phe Thr Arg Val Cys Val Phe Thr Val 290 295 300 Phe Leu Leu Thr Met Phe Gly Ala Ile Gly Cys Glu Leu Gln Ile Ile 305 310 315 320 Arg Lys Lys Leu Gln Arg Ala Ala Asn Ser Pro Arg Ile Val Leu Gly 325 330 335 Val Cys Ala Cys Gly Asn Leu Leu Met Ala Val Val Phe Phe Ser Leu 340 345 350 Asn Lys Val Glu Leu Val Ala Leu 355 360 117 394 PRT Japanese Macaque Herpesvirus 117 Met Pro Val Ser Phe His Tyr Gly Ala Arg Val Asp Val Asp Ala Leu 1 5 10 15 Gly Asn Ile Ser Lys Val Tyr Asp His Ile Lys Gly Ile Val Lys Lys 20 25 30 Gly Val Ile Gln Ile Ser Gly Gln Gly Arg Ala Pro Val Leu Ser Val 35 40 45 Leu Ser Ser Val Gly Asp Ala Gly Val Leu Gly Leu Arg Leu Lys Asn 50 55 60 Ala Leu Ala Pro Leu Met Val Tyr Ser Asp Met Thr Asp Glu Val Ser 65 70 75 80 Phe Ser Phe Arg Asn Thr Ser Leu Gly Asn Thr Phe Thr His Thr Arg 85 90 95 Glu Met Phe Gly Val Asn Ile Thr Glu Met Asn Val Ala Phe Tyr His 100 105 110 His Gly Asp Glu Ser Asn Ala Glu Gly Lys Pro Gln Phe Val Arg Thr 115 120 125 Thr Ile Ala Tyr Gly Asp Asn His Thr Ser Thr Val His Lys Ser Val 130 135 140 Val Asp Glu Pro Asn Leu Pro Ser Phe His Asp Arg Leu Glu Gln Ala 145 150 155 160 Gly Thr Gly Asn Arg Leu Phe Leu Thr Val Lys Thr Leu Thr Leu Leu 165 170 175 Ser Lys Trp Leu Arg Gln Gln Lys Thr Arg Ala Lys Gln Val Val Thr 180 185 190 Val Ser Leu Ser Glu Thr Leu Ala Val Ala Thr Phe Thr Val Asp Gly 195 200 205 Val Ser Lys Ile Ile Asp Phe Lys Pro Asp Thr Pro Asp Ala Lys Trp 210 215 220 Thr Cys Ala Lys Gly Arg Lys Leu Asp Val Gly Val Val Ser Ser Asp 225 230 235 240 Leu Thr Thr His Val Ser Leu Glu Ser Leu Val Ala Ala Leu Asn Ala 245 250 255 Cys Lys Ile Pro Gly Phe Phe Leu Pro Gly Phe Arg Trp His Ala Asn 260 265 270 Glu Ile Leu Glu Val Glu Gly Leu Pro Leu Thr Asp Ser Leu Ala Asp 275 280 285 Val Lys Leu Gly Val Met Leu Leu Lys Val Asp Pro Thr Asp Arg Asn 290 295 300 Asn Ala Val Pro Gly Asn Leu Ser Glu Gly Ala Asp Pro Glu Gly Val 305 310 315 320 Pro Glu Leu Pro Ser Pro Pro Arg Thr Pro Asp Leu Asp Leu Lys Glu 325 330 335 Gln Cys Val Pro Asn Ala Glu Asp Gly Thr Glu Pro Thr Asp Gly Gly 340 345 350 Ala Lys Ser Leu Arg Thr Ser Gly Ser Arg Pro Glu Lys Lys His Gly 355 360 365 Lys Arg Lys His Ser Ser Ser Pro Ser Arg Gly Lys Ala Lys Thr Lys 370 375 380 Thr Pro Arg Ala Thr Phe Asn Pro Leu Phe 385 390 118 80 PRT Japanese Macaque Herpesvirus 118 Met Leu Thr Pro Asn Ile Ser Arg Val Trp Val Asn Val Phe Pro Arg 1 5 10 15 Glu Val Phe Arg Lys Leu Lys Leu Thr Ser Ser Val Met Ser Glu Tyr 20 25 30 Thr Ile Ser Gly Ala Ser Ala Phe Leu Ser Arg Arg Pro Arg Thr Pro 35 40 45 Ala Ser Pro Thr Leu Glu Ser Thr Leu Arg Thr Gly Ala Leu Pro Trp 50 55 60 Pro Leu Ile Cys Ile Thr Pro Phe Leu Thr Met Pro Leu Met Trp Ser 65 70 75 80 119 314 PRT Japanese Macaque Herpesvirus 119 Met Ser Gly Leu Ser Ile Val Thr Ala Ala Met Glu Ser Pro Asp Arg 1 5 10 15 Phe Leu Tyr Ala Ser Asp His Pro Gly Phe Leu Ala Leu Thr Gln Glu 20 25 30 Thr Trp Gln Asn Arg Trp Phe Pro Ser Gln Ile Ser Leu His Glu Asp 35 40 45 Ser Asp Glu Val Arg Leu Leu Ser Pro Thr Asp Arg Glu Phe Tyr Gln 50 55 60 Phe Leu Phe Thr Phe Leu Gly Met Ala Glu Ser Leu Val Asn Phe Asn 65 70 75 80 Ile Glu Asp Leu Val Lys Glu Phe Ser Asn His Asp Val Thr His Tyr 85 90 95 Tyr Ala Glu Gln Val Ala Met Glu Asn Ile His Gly Lys Val Tyr Ala 100 105 110 Asn Ile Leu Asn Leu Phe Phe Gly Gly Asn Arg Gly Asp Leu Met Thr 115 120 125 Tyr Ala Lys Lys Ile Val Glu Asp Ala Thr Leu Ala Lys Lys Ile Asp 130 135 140 Trp Leu His Ser Arg Val Arg Lys Ala Thr Thr Arg Ala Glu Lys Val 145 150 155 160 Leu Leu Phe Leu Val Ile Glu Gly Ile Tyr Phe Ile Ser Ser Phe Tyr 165 170 175 Ser Ile Gly Leu Phe Arg Leu Arg Gly Val Met Arg Gly Val Cys Leu 180 185 190 Ala Asn Asp Tyr Ile Ser Arg Asp Glu Leu Leu His Thr Arg Ala Ala 195 200 205 Gly Leu Leu Tyr Asn Thr Met Ile Ser Arg Asp Glu Ser Pro Ser Val 210 215 220 Ala Tyr Ile His Gly Leu Phe Arg Glu Ala Val Glu Ile Glu Thr Leu 225 230 235 240 Phe Ile Arg Ser Lys Ser Arg Gly Val Thr Met Val Asn Val Gly Asp 245 250 255 Ile Glu Gln Phe Leu Gln Ala Thr Ala Asp Arg Ile Leu Lys Ser Ile 260 265 270 Asn Val Pro Pro Leu Phe Gly Ala Arg Pro Pro Asn Ala Cys Pro Leu 275 280 285 Ser Tyr Thr Ser Ala Lys Ser Val Asn Phe Phe Glu Arg Asp Asn Ser 290 295 300 Glu Tyr Val Thr Ser Val His Asn Asp Leu 305 310 120 788 PRT Japanese Macaque Herpesvirus 120 Met Asn Thr Glu Thr Ser Phe Ser Ala Ala Lys Ser Ala Lys Pro Leu 1 5 10 15 Thr Leu Val Thr Asn Ala Glu Thr Gly Gly Cys Ser Ser Ser Leu Asp 20 25 30 Pro Glu Arg Cys Ala Glu Ser Leu Val Asn Ser Leu Lys Ala Thr Leu 35 40 45 Gly Trp Asp Val Glu Ala Asn Ser Leu Thr Gly Leu Leu Trp His Arg 50 55 60 Ile Met Glu Asp Arg Cys Leu Val Thr Val Lys Asp Tyr Leu Thr Val 65 70 75 80 Phe Gly Glu Lys Leu Ser Asp Glu Val Arg Glu Phe Met Leu Lys His 85 90 95 Glu Ala Ala Leu Asp Gly Leu Leu Gln Asp Phe Lys Gln Ser Lys Ala 100 105 110 Tyr Ala Asn Leu Val Asn Cys Gly Tyr Leu Ser Ala Val Arg Phe Tyr 115 120 125 Asp Thr Tyr Val Leu Arg Thr His Gly Ser Ser Pro Ile Phe Glu Ser 130 135 140 Val Ala Gln Met Phe Met Arg Val Ala Val Phe Val Ala Cys Gln Cys 145 150 155 160 Ile Lys Phe Pro Cys Leu Arg Lys Thr Leu Arg His Leu Val Gln Ser 165 170 175 Glu Thr Glu Leu Asp Glu Met Tyr Leu Val Gly Tyr Ala Phe His Tyr 180 185 190 Ile Ser Ser Gln Ile Val Cys Cys Ala Thr Pro Val Leu Arg Ser Ala 195 200 205 Gly Leu Arg Gly Gly Gln Leu Ser Ser Cys Phe Ile Leu Lys Pro Ser 210 215 220 Met Ala Thr Glu Asn Lys Thr Leu Lys Ala Leu His Glu Glu Met Ser 225 230 235 240 Pro Leu Leu Ala Ser Lys Ser Gly Val Gly Ile Asp Val Ser Ser Phe 245 250 255 Ala Glu His Lys Asn Ile Thr Ser Cys Leu Lys Leu Ile Asn Ala His 260 265 270 Val Gly Tyr Phe Asn Asp Asn Asn Ile Arg Pro Val Gly Ala Ser Ala 275 280 285 Tyr Met Glu Leu Trp His His Gln Ile Cys Asp Phe Leu Asn Ala Lys 290 295 300 Met Pro Glu Asn Gln Glu Arg Cys His Asn Leu Phe Gln Gly Val Cys 305 310 315 320 Val Pro Glu Leu Phe Phe Arg Leu Tyr Glu Thr Asn Pro Asp Gly Gln 325 330 335 Trp His Leu Phe Ala Pro Glu Val Ala Pro Asn Leu Leu Lys Leu Tyr 340 345 350 Gly Ala Glu Phe Glu Ile Glu Tyr Asn Arg Leu Val Ala Ala Gly Lys 355 360 365 His Ser Ser Ser Leu Pro Leu Lys Ser Met Met Tyr Ala Leu Ile Asn 370 375 380 Thr Val Ile Lys Thr Gly Ser Pro Tyr Val Leu Leu Lys Glu Ala Leu 385 390 395 400 Asn Lys His His Trp Cys Glu Thr Gln Gly Ser Ala Ile Asn Cys Ser 405 410 415 Asn Leu Cys Ala Glu Ile Val Gln Gln Pro Glu Gly Gln Ala Ser Val 420 425 430 Cys Asn Leu Ala Asn Ile Ser Leu Pro Lys Cys Leu Arg Pro Pro Arg 435 440 445 Gly Lys Ser Gly Val Glu Pro Gly Lys Gly Asp Val Thr Phe Gly Phe 450 455 460 Glu Leu Leu Asp Asp Ala Val Glu Ala Ala Val Ile Ile Val Asn Ala 465 470 475 480 Cys Ile Leu Gly Gly Thr Ala Pro Thr Glu Ser Val Arg Arg Gly Gln 485 490 495 Lys Glu Arg Ser Met Gly Ile Gly Val Gln Gly Leu Ala Asp Val Phe 500 505 510 Ala Glu Leu Gly Phe Gly Tyr Leu Asp Ala Glu Ser Ala Lys Leu Asp 515 520 525 Val Glu Ile Phe Gln Ala Met Tyr Phe Ala Ala Val His Thr Ser His 530 535 540 Glu Ile Val Leu Leu Gly Glu Gly Thr Pro Phe His Gly Trp Glu Arg 545 550 555 560 Ser Arg Leu Ala Gln Gly Val Phe His Trp Gln Thr Trp Asp Gly Val 565 570 575 Lys Pro Ser His Pro Pro Leu Glu Arg Trp Glu Gln Leu Gly Arg Ser 580 585 590 Ile Ala Gln His Gly Ile Phe Asn Ser Gln Phe Leu Ala Leu Met Pro 595 600 605 Thr Ala Gly Thr Ser Gln Leu Thr Gly Tyr Thr Glu Ala Phe Tyr Pro 610 615 620 Phe Phe Ala Asn Ile Ala Ser Lys Val Thr Ser Lys Glu Glu Ile Leu 625 630 635 640 Lys Pro Asn Val Thr Phe Phe Lys Arg Val Lys Pro Gly Asp Leu Arg 645 650 655 Thr Val Arg Arg Tyr Gly Gly Asp Val Ala Ser Phe Pro Glu Pro Leu 660 665 670 Lys Asp Arg Tyr Lys Ile Phe Leu Thr Ala Phe Asp Tyr Cys Pro Ile 675 680 685 Lys Gln Leu Glu Arg Ala Gly Ala Arg Ala Pro Phe Val Asp Gln Ser 690 695 700 Gln Ser Leu Asn Phe Phe Leu Lys Glu Glu Gln Ala Thr Arg Ala Ser 705 710 715 720 Tyr Ile Arg Asp Leu Leu Leu Thr Gly Tyr Arg Leu Gly Leu Lys Thr 725 730 735 Met Leu Tyr Tyr Cys Arg Ile Gln Lys Gln Thr Lys Leu Asn Ala Leu 740 745 750 Gln Cys Leu Asp Gln Val Val Gly Asp Asn Thr Ser Ser Glu Gly Ala 755 760 765 Glu Ser Asn Arg Val Gln Lys Ala Asp Gly Glu Gln Ala Glu Val Cys 770 775 780 Leu Ala Cys Gln 785 121 138 PRT Japanese Macaque Herpesvirus 121 Met Thr Pro Trp Arg Pro Gln Leu Leu Leu Ser Met Arg Ala Phe Trp 1 5 10 15 Ala Gly Arg Arg Leu Pro Arg Ala Leu Gly Ala Ala Arg Arg Asn Asp 20 25 30 Gln Trp Ala Leu Ala Ser Lys Asp Trp Pro Thr Cys Leu Pro Asn Ser 35 40 45 Ala Leu Ala Thr Leu Thr Pro Arg Ala Pro Ser Trp Thr Trp Arg Phe 50 55 60 Phe Arg Gln Cys Ile Leu Arg Arg Cys Thr Arg Val Thr Arg Leu Phe 65 70 75 80 Tyr Leu Ala Arg Gly Leu Arg Phe Met Asp Gly Ser Gly Val Asp Trp 85 90 95 Leu Arg Val Cys Phe Thr Gly Lys Arg Gly Thr Ala Leu Ser Arg Pro 100 105 110 Thr Arg Pro Trp Lys Asp Gly Ser Ser Trp Gly Ala Ala Ser Pro Ser 115 120 125 Met Glu Phe Ser Thr Ala Ser Phe Trp Arg 130 135 122 97 PRT Japanese Macaque Herpesvirus 122 Met Glu Arg Val Thr Asn Gln Val His Leu Val Gln Leu Arg Phe Thr 1 5 10 15 Leu His Gln Val Ser Glu Gly Leu Pro Gln Thr Arg Lys Phe Tyr Ala 20 25 30 Leu Thr Gly His Lys Asn Ser His Pro His Lys His Leu Gly Asn Ala 35 40 45 Leu Lys Asn Gly Arg Arg Ala Met Gly Ser Gln His Val Arg Ile Val 50 55 60 Lys Pro Asp Gly Arg Gln Val Ala Ala Val Asn Glu Ile Cys Val Cys 65 70 75 80 Leu Ala Leu Leu Lys Val Leu Gln Lys Thr Val Lys Gly Arg Phe Val 85 90 95 Phe 123 331 PRT Japanese Macaque Herpesvirus 123 Met Lys Thr Arg Asp Ala Asn Val Asn Lys Leu Asn Asp Ser Leu Met 1 5 10 15 Arg Leu Leu Pro Pro Pro Pro His Arg Val Ser Leu Ser Arg Gly Arg 20 25 30 Asp Phe Ser Lys Gly Val Arg Asp Leu Leu Ser Lys Tyr Val Val Ser 35 40 45 Thr Thr Thr Gly Val Glu Ala Ile Lys Asp Gly Phe Leu Ser Val Ser 50 55 60 Pro Lys Cys Gln Thr Tyr Gly Asp Phe Leu Ile Tyr Ser Gln Thr Met 65 70 75 80 Ser Ser Gln Glu Pro Arg Gly Thr Tyr Leu Phe Ser Phe Lys Gln Thr 85 90 95 Asp Thr Gly Ser Ser Ile Asp Met Leu Phe Thr Pro Thr Ser Leu Ala 100 105 110 Arg Leu Ser Arg Met Asp Ala Asp Ser Ala Pro Gln Thr Asn Arg Ile 115 120 125 Ala Cys Val Trp Tyr Gly His Glu Ser Gly Leu Leu Asp Ala Ile Pro 130 135 140 Asn Phe Glu Glu Leu Leu Glu Thr Gly Ser Leu His Gln Phe Leu Ala 145 150 155 160 Pro Val Gly Pro Leu Val Gln Thr Val His Ser Thr Phe Val Thr Lys 165 170 175 Val Thr Ser Ala Leu Lys Gly Asp Val Val Ala Arg Glu Pro Val Val 180 185 190 Thr His Ile Gly Leu Thr Leu Pro Ser Asp Met Phe Val Asp Leu Asp 195 200 205 Asp Ser Cys Pro Ser Ser Leu Arg Asp Glu Pro Leu Pro Ala His Ser 210 215 220 Ser Ile Tyr Val Cys Leu Thr Tyr Ile Arg Ala Asn Asn Arg Pro Ala 225 230 235 240 Leu Gly Leu Gly Phe Phe Lys Ser Gly Lys Gly Tyr Cys Glu Ile Ala 245 250 255 Ala Gln Leu Arg Asp Phe Tyr Ser Gly Val Ile Arg Thr Lys Tyr Ile 260 265 270 Gln Leu Gln Asn Asp Leu Tyr Ile Asn Arg Leu Ala Phe Gly Val Val 275 280 285 Cys Arg Leu Gly Ser Val Pro Ser Gly Ser Gln Pro Ser Phe Gln Ser 290 295 300 Leu His Phe Lys Gly Ala Ala Leu Pro Val Leu Lys Phe Thr Glu Phe 305 310 315 320 Val Ser Asn Pro Gly Ser Trp Lys Leu Phe Leu 325 330 124 939 PRT Japanese Macaque Herpesvirus 124 Met Thr Ser Ser Ile Ser Ala Ala Arg Ala Asp Asn Gly Asp Glu Asn 1 5 10 15 Thr Gly Gly Leu Tyr Arg Leu Ile Asp Asn Leu Leu Thr Cys Thr Gly 20 25 30 Ser Leu Gln Gln Leu Lys Leu Leu Met Glu Phe Gln Leu Lys Pro Leu 35 40 45 Pro Thr Ala His Leu Leu Ser Met Pro Thr Val Thr Arg Phe Leu Asn 50 55 60 Thr Ala Phe Lys Ile Asp Asn Pro Leu Val Ser Phe Ile Gln Lys His 65 70 75 80 Pro Val Phe Phe Leu Met Arg Val Ala Arg Leu Pro Asp Pro Val Ile 85 90 95 Thr Asp His Gln Ser Ala Glu Thr Ser Thr Gly Ile Leu Ser Glu Val 100 105 110 Val Asn Val Leu Asn Ile Ala Ile Gln Lys Pro His Glu Ser Pro Ala 115 120 125 Ala Lys Asp Asp Asp Tyr Leu Asp Asn Arg Ala Ile Leu Thr Met Ile 130 135 140 Thr Glu Tyr Ile His His Val Thr Ser Arg Thr Pro Ser Gly Ile Pro 145 150 155 160 Pro Thr Pro Pro Met Gly Ile Ser His Leu Pro Cys Val Glu Gln Ile 165 170 175 Leu His Glu Thr His Arg Gln Tyr Trp Asn Leu Ala Leu Pro Glu Ser 180 185 190 Leu Phe Ile Asp Thr Gly Glu Val Ala Ser Pro Leu Gln Thr Trp Leu 195 200 205 Ile Ile Ser Tyr Cys Lys Lys Leu Gln Leu Ala Pro Pro Pro Leu Phe 210 215 220 Pro Pro Ala Asp Glu Leu Ala Arg Arg Leu Val Thr Gly His His Glu 225 230 235 240 Leu Phe Val Pro Leu Ser Thr Ser Leu Glu Thr Tyr Ile Thr Met Pro 245 250 255 Val Ser Lys Arg Arg Ala Phe Glu Ile Tyr Ser Val Phe Ala Lys Ser 260 265 270 Lys Asn Ile Val Asp Gly Thr Pro Ile Leu Ala Phe Thr Asp Thr Glu 275 280 285 Leu Thr Thr Phe Thr Pro Glu Leu Leu Phe Leu Tyr Asp Phe Val Ile 290 295 300 Glu Ser Leu Cys Lys Asn Gln Ala Tyr Gly Cys Ser Arg Asn Ala Ile 305 310 315 320 Glu His Phe Ile Lys Lys Gly Ile Asp Phe Met Ala Glu Leu Gly Ala 325 330 335 Phe Ile Glu Lys Thr Cys Gly Tyr Arg Ser Thr Val Ser Leu Ser Asn 340 345 350 Val Arg Ser Val Lys Ala Arg Leu Ala Ser Cys Gly Leu Ser Lys Glu 355 360 365 Ala Cys Glu Asp Phe Arg Thr Met Ile Leu Met Thr Pro His Glu Thr 370 375 380 Thr Pro Lys Trp Glu Asn Phe Thr Asp Phe Leu Glu Met Val Asn Gln 385 390 395 400 Leu Thr Leu Tyr Gly Phe Tyr Phe Tyr Glu Cys Leu Asn Gln Tyr Ser 405 410 415 Pro Thr Ser Ile Ser Leu Ala Lys Ile Gln Asn Ile Leu Asn Arg Val 420 425 430 Asp Ala Glu Gln Ser Asp Arg Ala Leu Trp Arg Thr Pro Leu Ile Gly 435 440 445 Ser Phe Pro Phe Pro Trp Lys Leu Asn Asn Val Leu Ala Phe Phe Lys 450 455 460 Pro Ser Ala Pro Val Ala Thr Leu Gln Lys Ile Tyr Lys Ala Ile Pro 465 470 475 480 Ser Tyr Leu Met Arg Ser Leu Phe Glu Ile Ala Ala Asn Lys Ser Trp 485 490 495 Gly Asn Ile Ala Leu Ala Glu Arg Ala Pro Leu Thr Asp Ile Gln Thr 500 505 510 Ala Glu Pro Asp Gln Gly Pro Val Pro Thr Gln Val Ile Ala Lys Tyr 515 520 525 Cys Ser Arg Leu Gln Ile Ser Ala Thr Asp Tyr Asp Ala Val Ile Val 530 535 540 Ser Ser Pro Gly Phe Ala Thr Glu Phe Ile Arg Thr Lys Leu Tyr Pro 545 550 555 560 Ile Leu Ser Glu Val Leu Arg Asn Thr Ser Lys Lys Asn Arg Ser Leu 565 570 575 Phe Gln Leu Arg Trp Leu Ile Val Phe Ala Ala Glu Asp Ala Lys Asp 580 585 590 Leu Ala Pro Ile Arg Arg Ser Leu Ala Leu Ala Tyr Phe Gln Ile Met 595 600 605 Asp Ile Leu Glu Glu Lys His Ser Pro Glu Ser Phe Tyr Asn Leu Leu 610 615 620 Asp Tyr Leu Gln Asp Thr Phe Arg Cys Ile Arg Gln Val Ile Pro Glu 625 630 635 640 Ala Thr Cys Pro Gln Glu Phe Leu Gln Tyr Leu Phe Thr Phe Gln Asn 645 650 655 Leu Pro Ile Ala Ala Ser Phe Ile Gln Thr Ser Met Thr Phe Val Asp 660 665 670 Asp Leu Asn Asn Gly Ile Pro Gly Ile Leu Asp Leu Val Ser Leu Gly 675 680 685 Ala Ala Phe Tyr Asn Met Lys Leu Leu Tyr Asp Ser Thr Leu Asp Thr 690 695 700 Val Glu Ile Pro Thr Glu Glu Gly Gln Pro Ile Val Val Ser Met Phe 705 710 715 720 Val Phe Lys Ser Thr Ile Arg Ile Leu Glu Lys Leu Leu Gln Glu Ala 725 730 735 Val Ile Ala Leu Ala Gln Thr Ser Glu Pro Met Tyr Ala Ala His Ile 740 745 750 Arg Leu Met Gln His Leu Thr Tyr Met Gln Lys Ile Ala Gly His Glu 755 760 765 Ile Met Thr Thr Gln Leu Pro Ser Val Phe His Glu Ile His Glu Gly 770 775 780 Tyr Leu Gln Cys Phe Lys Arg Phe Lys Arg Leu Met Leu His Val Thr 785 790 795 800 Gly Ser Cys Cys Tyr Ser Leu Thr Arg Tyr Phe Gly Phe Leu Tyr Gln 805 810 815 Pro Pro Leu Ile Pro Asp Thr Ile Val Gln Lys Ile Leu Asn Phe Asn 820 825 830 Asp Lys Thr Asp Thr Thr Asp Asp Ile Leu Lys Ser Leu Ser Gln Pro 835 840 845 Val Gly Gln Glu Pro Leu Ser Ala Glu Asn Glu Ser Ser Ser Arg Leu 850 855 860 Ser Lys Asn Asp Val Glu Leu Leu Gln Lys Leu Tyr Asp Asp Phe Arg 865 870 875 880 Asn Gly Ser Thr Asn Asp Asn Pro Thr Ser Ile Lys Leu Glu Tyr Ser 885 890 895 Gly Asn Tyr Asn Glu Thr Gln Val Ser Val Asp Trp Ser Thr Tyr Asn 900 905 910 Leu Val Thr Tyr Thr Ala Pro Asp Asp Thr Leu Lys Phe Thr Pro Val 915 920 925 Asn Thr Glu Ala Leu Asp Arg Met Leu Ala Glu 930 935 125 1966 PRT Japanese Macaque Herpesvirus 125 Met Glu Leu Pro Pro Ile Phe Ser Lys Phe Lys Ile Glu Gly Val Ala 1 5 10 15 Thr Thr His Gln Ala Asp Cys Arg Phe Gly Gln Tyr Ala Gly Ser Gln 20 25 30 Cys Leu Ser Asn Cys Val Ile Tyr Leu Ala Gln Ser Tyr Phe Asn Arg 35 40 45 Glu Ser Pro Val Thr Asp Thr Asn Asp Leu Asp Asp Val Leu Arg Gln 50 55 60 Gly Ala Thr Leu Asp Phe Ile Leu Arg Arg Ser Gly Thr Leu Gly Tyr 65 70 75 80 Asn Gln Tyr Ala Gln Leu His His Ile Pro Ser Phe Ile Lys Thr Asn 85 90 95 Glu Trp Ser Ala Ala Ile Phe Gln Ser Gln Glu Tyr Phe Gly Leu Ile 100 105 110 Gly Leu Asp Ala Ala Ile Arg Glu Pro Phe Ile Glu Ser Leu Lys Ser 115 120 125 Ile Leu Thr Arg Asn Tyr Ala Gly Thr Val Gln Tyr Phe Leu Phe Ile 130 135 140 Cys Gly Asp Lys Ala Gly Ala Val Ile Ile Lys Asn Lys Thr Phe Tyr 145 150 155 160 Leu Phe Asp Pro His Cys Val Pro His Val Pro Asn Ser Pro Ala His 165 170 175 Val Ile Ser Ser Ala Asp Pro Thr Ala Ile Leu Glu Tyr Val Ser Pro 180 185 190 Pro Asp Arg Glu Tyr Thr Gly Ser Phe Leu Tyr Ile Met Pro Ser Glu 195 200 205 Tyr Val Asn Pro Glu His Tyr Ile Thr Asn His Tyr Arg Thr Ile Thr 210 215 220 Phe Ala Lys Val His Gly Pro Gln Ile Asp Ile Ser Thr Gly Ile Glu 225 230 235 240 Pro Cys Thr Ile Glu Asp Ile Pro Ser Pro Pro Arg Ser Pro Asp Val 245 250 255 Thr Ser Lys Ser Ser Asn Leu Ala Arg Val Pro Lys Thr Thr Thr Asp 260 265 270 Thr Ser Ser Ala Lys Thr Thr Pro Ala Pro Leu Ser Gly Leu Leu Gly 275 280 285 Val Glu Pro Pro Thr Ser Tyr Pro Asp Pro Ala Ala Asp Asp Ala Asp 290 295 300 Thr Lys Leu Leu Thr Pro Ala Pro Ala Arg Thr Ala Val Asp His Pro 305 310 315 320 Glu Phe Gln Thr Thr Pro Gly Ala Thr Leu Leu Leu Ser Glu Leu Ser 325 330 335 Ala Ser Arg Gly Arg Lys Arg Lys Leu Ser Ser Leu Gln Arg Tyr Ser 340 345 350 Asp Ser Asp Glu Ala Ser Ser Asp Asp Glu Gly Ala Pro Arg Arg Arg 355 360 365 Ala His Asp Asp Ala Ile Ser Ala Glu Val Ile Trp Met Asp Asp Asp 370 375 380 Ile Ser Pro Leu Tyr Ser Pro Ser Ala Thr Pro Ser Phe Asp Asp Val 385 390 395 400 Phe Asp Ser Pro Pro Met Ser Pro Glu Phe Thr Tyr Thr Asn Ala Thr 405 410 415 Glu Asp Thr Asp Gly Ala Phe Leu Glu Gln Ile Val Arg Asp Ala Glu 420 425 430 Thr Pro Phe Ser Ala Phe Asn Asp Leu Ile Ser Asp His Asp Phe Ser 435 440 445 Ser Leu Asp Lys Lys Ile Glu Gln Leu Ile Lys Tyr Glu Ala Pro Ser 450 455 460 Gln His Leu Pro Asn Ile Ser Asp Lys Arg Asn Gly Arg Ala Val Arg 465 470 475 480 Glu Ala Ala Ala Leu Gln Ala Met Asp Lys Ile Met Ile Asn Ile Ile 485 490 495 Leu Glu His Gly Leu Ile Thr Asp Ala Gln Ala Arg Gly Pro Ser Ala 500 505 510 Cys Lys Asn Val Leu Gln Phe Phe Ile Leu Trp Gly Glu Lys Leu Asn 515 520 525 Ile Pro Ile Ser Asp Ala Lys Gln Val Leu Glu Leu Asp Leu Gln Leu 530 535 540 Ile Pro Leu His Thr Ala Leu Ser Glu Gly Lys Phe Lys Gln Gly Ala 545 550 555 560 Phe Lys Lys His Leu Thr Thr Lys Ile Asn Arg Cys Leu Ala Ser Met 565 570 575 Arg Ala Thr His Ala Asn Ala His Lys Lys Leu Ala Ser Ala Phe Asn 580 585 590 Ile Glu Gly Ser Gln Ile Ser Ser Ser Glu Thr Lys Ile Ser Val Arg 595 600 605 Ala Leu Lys Glu Gln Ile Ala Asn His Leu Ser Pro Gly Phe Leu Ala 610 615 620 Val Tyr Ser Ala Asp Glu Leu Lys His Leu Arg Asp Lys Ile Arg Asp 625 630 635 640 Leu Lys Thr Gly Ile Glu Gln Arg Asn Arg Glu Ile Gln Gln Glu Glu 645 650 655 Leu Phe Phe Gly Ala Val Leu Thr Ala Leu Asp Thr Phe Gln Pro Pro 660 665 670 Pro Lys Pro Ala Tyr Pro Met Glu Ile Phe Pro His Arg Lys Thr Asp 675 680 685 Val Met Leu Asn His Leu Ala Ser Ile Thr Thr Arg Leu Thr Asp Asp 690 695 700 Ala Thr Glu Ala Leu Asn Asn Tyr Leu Glu Thr Pro Pro Asp Gln Gly 705 710 715 720 Thr His Ile Thr Asn Ile Pro Asn Phe Ser Ser Ile Val Ala Asn Ile 725 730 735 Ile Ser Thr Ile Lys Ile Leu Thr Tyr Ala Glu Asn Asp Met Gln Leu 740 745 750 Asn Val Thr Pro Met Ala Thr Tyr Arg Arg Gln Leu Leu Tyr Leu Gly 755 760 765 Gly Glu Leu Ala Thr Ile Phe Asn Leu Glu Trp Pro Tyr Glu Thr Val 770 775 780 Pro Pro Val Gln Glu Leu Pro Leu Val Ala Arg Ala Lys Ala Lys Met 785 790 795 800 Glu Ser Val Thr Lys Met Glu Lys Asn Gln Gln Ala Leu Asp Gln Ile 805 810 815 Leu Gly Asp Ala Glu Thr Leu Leu Asp Thr Ile Thr Ala Thr Ser Gly 820 825 830 Asn Glu Asn Pro Val Arg Ala Met Ser Ile Pro Ile Leu Glu Thr Tyr 835 840 845 Ile Thr Asn Ala Gly Ala Leu Ile Gly Thr Ser Arg Asn Pro Arg Phe 850 855 860 Glu Lys Leu Lys Ala Ala Ile His Asp Leu Ala Ser Ser Glu Ser Phe 865 870 875 880 Ile Ile Met Leu Leu Asn Asn Thr Arg Leu Asp Asn Ile Ser Asp Asn 885 890 895 Leu Ala Lys Ile Asp Gly Ile Leu Thr Asn Asn Thr Arg Phe Leu Ser 900 905 910 Thr Ala Thr Val Thr Lys Thr Leu Gln Thr Leu Gly Ser Ser Leu Ile 915 920 925 Arg Glu Cys Val Glu Ala Leu Asp Lys Arg Ser Pro Ser Ser Leu Thr 930 935 940 Asp Ala Arg Leu Leu Ala Val Gln Thr Ile Leu Gly His Ala Ser Val 945 950 955 960 Pro Asp His Glu Thr Leu Thr Arg Ile Val Ser Gly Val Ala Ser Ala 965 970 975 Gln Lys Glu Ser Ala Gly Asp Asp Pro Asp Arg Trp Thr Arg Val Thr 980 985 990 Gly His Leu Asn Glu Leu Lys Leu Ala Ala Thr Gln Ser Asn Val Asp 995 1000 1005 Lys Ala Thr Arg Arg Lys Leu Leu Met Ile Ile Thr Arg Asp Leu 1010 1015 1020 Lys Glu Ala Glu Val Ser Gln Glu Thr Val Leu Glu Thr Arg Trp 1025 1030 1035 Gln Glu Asn Val Leu Lys Phe Gln Pro Ser Thr Ser Lys Glu Ile 1040 1045 1050 Glu Asp Phe Leu Gln Ser Ala Pro Ser Ala Lys Ala Arg Lys Phe 1055 1060 1065 Ala Glu Lys His Leu Arg Thr Leu Ile Ala Gln Phe Asp Gly His 1070 1075 1080 Glu Gln Arg Pro Ser Glu Ala Thr Ala Val Pro Met Asp Tyr Thr 1085 1090 1095 Pro Thr Pro Ile Pro Thr Pro Gln Ala Val Ser Thr Ala Thr Ala 1100 1105 1110 Glu Lys Gly Lys Ala Ala Trp Asn Lys Ile Gln Gln Ala Phe Gln 1115 1120 1125 Asp Phe Asn Phe His Leu Ile Asp Ala Ser Asp Trp Gln Glu Met 1130 1135 1140 Ala Ser Glu Tyr Ser Arg His Gly Ser Ser Leu Pro Gly Thr Val 1145 1150 1155 Gly Pro Lys Leu Val Arg Phe Met Glu Ser Ile Ser Asn Thr Leu 1160 1165 1170 Asp Asp Ile Leu Thr Gln Lys Leu Ala Ser Leu Leu Pro Asn Gly 1175 1180 1185 Pro Ala Phe Arg Pro Pro Ala Phe Asp Trp Ile Ala Pro Tyr Gln 1190 1195 1200 Thr Arg Val Asn Ala Phe Leu Lys Thr Ile Gly Leu Pro Met Val 1205 1210 1215 Arg Asp Leu Ala Asp Lys Ile His His Gln Cys Gln Thr Val Ser 1220 1225 1230 His Ala Val Gln Ser Ala Asp Leu Gln Gln Ala Thr Val Gly Thr 1235 1240 1245 Ser Leu Glu Arg Pro Ala Ala Glu Tyr Cys Arg Ile Leu Ser Asp 1250 1255 1260 Met Gln Val Ala Phe Asn Asp His Gly Ile Ala Val Arg Ser Glu 1265 1270 1275 Ala Ala Ala Tyr Thr Asp Ala Ile Asn Ser Pro Ala Asn Val Ala 1280 1285 1290 Thr Pro Pro Lys Pro Asn Leu Glu Ala Pro Lys Lys Leu Met Thr 1295 1300 1305 Ala Thr Asp Val Leu Thr Val Glu Asp Phe Pro Glu Phe Leu Lys 1310 1315 1320 Thr Ser Ile Leu Gln Gln Glu Gln Arg Leu Ile Ala Leu Gln Arg 1325 1330 1335 Ala Glu Phe Gln Gln Leu Glu Ala Ser Ile Ser Ala Ala Glu Arg 1340 1345 1350 Leu Arg Gln Ser Thr Arg Asn Glu Ile Ala Gly Lys Met Ala Thr 1355 1360 1365 Ala Ile Thr Gln Leu Leu Pro Arg Ala Pro Val Ala Ile Ser Ser 1370 1375 1380 Arg Pro Leu Asn Leu Ser Lys Pro Ile Asp Phe Leu Ser Ser Thr 1385 1390 1395 Val Tyr Asp Lys Ile Leu Asp Lys Glu Pro Tyr Glu Thr Ala Ile 1400 1405 1410 Ala Gly Phe Ala Trp Leu Glu Thr Ala Thr Lys Ser Val Met Val 1415 1420 1425 Tyr Ser His Gln Asn Gln Thr Gln Gln Leu Asn Val Leu Leu Ser 1430 1435 1440 Glu Val Glu Lys Gln Ser Thr Ile Ala Gln Arg Leu His Asp Leu 1445 1450 1455 Glu Val Ser Ala Arg Asn Thr Asp Asp Val Lys Val Leu Lys Gln 1460 1465 1470 Ala Leu Asp Glu Leu Ala Pro Leu Arg Val Lys Gly Gly Lys Thr 1475 1480 1485 Thr Val Asp Ala Trp Lys Gln Lys Leu Glu Ser Ile Glu Ser Leu 1490 1495 1500 Leu Arg Ala Thr Arg Thr Ala Gly Glu Ile Ser Ser Glu Leu Glu 1505 1510 1515 Arg Ile Gly Ala Gln Ala Val Gly Thr Ile Ala Val Arg Asp Leu 1520 1525 1530 Gly Thr Leu Ser Asp Gln Cys Arg Glu Ala Ala Asn Phe Leu Lys 1535 1540 1545 Gln Ala Ser Leu Pro Glu Gly Phe Ser Asp Ile Gly Thr Lys Leu 1550 1555 1560 Ser Glu Leu Gln Ala Tyr Ile Lys Tyr Lys Lys Gln Phe Leu Glu 1565 1570 1575 His Phe Glu Thr Thr Gln Pro Asn Val Phe Arg Arg Phe Pro Leu 1580 1585 1590 Ser Gln Asn Ile Thr Glu Asn Val Pro Ala Arg Leu Ala Met Asp 1595 1600 1605 Ser Met Ala Arg Leu Ala Asn His Leu His Val Arg Gly Ser Ala 1610 1615 1620 Pro His Phe Thr Thr Trp Ile Glu Thr Leu Pro Thr Val Asp Pro 1625 1630 1635 Glu Lys Pro Thr His Val Pro Ala His Gly Gly Ala Pro Leu His 1640 1645 1650 Arg Gln Ile Thr Tyr Ser Asn Val Leu Glu Ala Leu Phe Ser Leu 1655 1660 1665 Cys Ser Thr Thr Leu Thr Pro Val Pro Thr Ala Pro Gly Leu Glu 1670 1675 1680 Ile Ala Thr Arg Ala Arg Arg Gly Ala Glu Ala Ala Thr Trp Met 1685 1690 1695 Asp Arg Gln Trp Pro Asp Ile Ala Gln Thr Leu Gln Asp Val Leu 1700 1705 1710 Asp Thr Tyr Glu His Thr Thr Thr His Ala Asn Arg Asp Ala Thr 1715 1720 1725 Ser Asn Ala Phe Leu Ala Met Cys Val Phe Thr Gln Ile Ile Arg 1730 1735 1740 Gly Ala Ser Arg Ala Val Thr Leu Pro Lys Leu Pro Gly Thr Ala 1745 1750 1755 Val Asp Phe Pro Glu Glu Ile Val Leu Thr Pro Arg Glu Cys Thr 1760 1765 1770 Thr Leu Val Thr Ala Met Trp Pro Thr Leu Ala Ala Ala Ile Leu 1775 1780 1785 Arg Leu Lys Ser Tyr Ser Glu Ala Leu Gly Leu Met Ser Arg Phe 1790 1795 1800 Leu Pro Leu Met Phe Gln Ala Leu Pro His Leu Thr Leu Glu Ala 1805 1810 1815 Gln Val Gln Asn Gly Pro His Asn Thr Pro Pro Gln Val Arg Cys 1820 1825 1830 Phe Ala Arg Thr Glu Ala Ile Pro Tyr Phe Pro Ala Gln Trp Gln 1835 1840 1845 Ser Ala Asn Leu Glu Gln Ser Leu Trp Gly Gln Thr Asp Phe Leu 1850 1855 1860 Gln Ile Cys Asp Asn Asn Gln Arg Lys Ala Arg Val Ala Ala Val 1865 1870 1875 Thr Trp Ala Leu Thr Thr Ile Asn Gly Val Val Leu Asp Gln Leu 1880 1885 1890 Trp Ser Thr Phe Lys Pro Met Thr Ala Ala Ser Asp Asp Thr Tyr 1895 1900 1905 Val Asp Leu Val Lys Thr Leu His Leu Thr Thr Phe Gly Pro Arg 1910 1915 1920 Gly Pro Thr Pro Arg Arg Glu Thr Thr Thr Glu His Pro Pro Tyr 1925 1930 1935 Glu Tyr Gly Gln Pro Thr Gly Tyr Cys Ile Ser Gly Gln Ser Thr 1940 1945 1950 Thr Pro Val Gln Ala Ser Asn Thr Pro Gly Val Arg Phe 1955 1960 1965 126 121 PRT Japanese Macaque Herpesvirus 126 Met Glu Ser Pro Thr Val Asn Ile Glu Glu Ile Tyr Arg Arg Pro Ser 1 5 10 15 Arg Ser Pro Arg Arg Ile Ser His Arg Arg Val Arg Ala Tyr Val Gly 20 25 30 Pro Leu Arg Arg Gln Thr Thr Leu Arg Arg Asn Pro Asn Ile Ala Glu 35 40 45 Gly Trp Thr Ala Cys Val Ser Asp Pro Trp Met Pro Thr Val Leu Lys 50 55 60 Glu Val Ala Trp Leu Pro Val Leu Phe Gly Ile Arg Gly Gly Arg Arg 65 70 75 80 Arg Phe Ala Leu Glu Arg Glu Leu Arg Val Leu Cys Pro Arg Arg Arg 85 90 95 Leu Pro Gly Leu Gly Ser Leu Ser Val Val Arg Arg Pro Val Asp Arg 100 105 110 Ile Ala Val Pro Val Trp Phe Trp Arg 115 120 127 147 PRT Japanese Macaque Herpesvirus 127 Met Ile Leu Ile Ile Ile Leu Ser Ile Ala Trp Arg Ala Ala Ala Ser 1 5 10 15 Arg Thr Ala Arg Pro Phe Arg Leu Ser Glu Met Phe Gly Arg Cys Cys 20 25 30 Glu Gly Ala Ser Tyr Leu Ile Asn Cys Ser Ile Phe Leu Ser Arg Glu 35 40 45 Glu Lys Ser Trp Ser Asp Ile Arg Ser Leu Asn Ala Glu Asn Gly Val 50 55 60 Ser Ala Ser Arg Thr Ile Cys Ser Arg Asn Ala Pro Ser Val Ser Ser 65 70 75 80 Val Ala Phe Val Tyr Val Asn Ser Gly Leu Ile Gly Gly Leu Ser Asn 85 90 95 Thr Ser Ser Asn Asp Gly Val Ala Asp Gly Glu Tyr Arg Gly Asp Ile 100 105 110 Ser Ser Ser Ile Gln Ile Thr Ser Ala Asp Ile Ala Ser Ser Cys Ala 115 120 125 Arg Leu Arg Gly Ala Pro Ser Ser Ser Asp Asp Ala Ser Ser Glu Ser 130 135 140 Glu Tyr Arg 145 128 106 PRT Japanese Macaque Herpesvirus 128 Met Val Trp Thr Ala Arg Arg Arg Ala Ser Val Arg Glu Asp Gly Leu 1 5 10 15 Leu Leu Ser Ser Ala Ser Thr His Ser Arg Ile Arg Leu Leu Pro Ser 20 25 30 Val Trp Ser Val Phe Val Thr Val Ala Val Glu Arg Lys Arg Val Leu 35 40 45 Leu Val Arg Met Pro Ser Ile Leu Ala Arg Leu Ser Asp Met Leu Ser 50 55 60 Ser Arg Val Leu Phe Ser Ser Ile Ile Met Asn Asp Ser Asp Asp Ala 65 70 75 80 Arg Ser Trp Met Ala Ala Leu Ser Phe Ser Asn Arg Gly Phe Arg Glu 85 90 95 Val Pro Ile Arg Ala Pro Ala Phe Val Ile 100 105 129 92 PRT Japanese Macaque Herpesvirus 129 Met Ser Arg Cys Ser Cys Trp Arg Ile Asp Val Phe Arg Asn Ser Gly 1 5 10 15 Lys Ser Ser Thr Val Arg Thr Ser Val Ala Val Ile Ser Phe Leu Gly 20 25 30 Ala Ser Arg Leu Gly Phe Gly Gly Val Ala Thr Leu Ala Gly Glu Leu 35 40 45 Ile Ala Ser Val Tyr Ala Ala Ala Ser Asp Leu Thr Ala Ile Pro Trp 50 55 60 Ser Leu Lys Ala Thr Cys Met Ser Glu Ser Ile Arg Gln Tyr Ser Ala 65 70 75 80 Ala Gly Arg Ser Lys Leu Val Pro Thr Val Ala Cys 85 90 130 97 PRT Japanese Macaque Herpesvirus 130 Met Val Pro Thr Ala Cys Ala Pro Met Arg Ser Ser Ser Glu Asp Ile 1 5 10 15 Ser Pro Ala Val Leu Val Ala Arg Ser Arg Asp Ser Met Leu Ser Ser 20 25 30 Phe Cys Phe His Ala Ser Thr Val Val Phe Pro Pro Phe Thr Leu Arg 35 40 45 Gly Ala Ser Ser Ser Ser Ala Cys Phe Ser Thr Phe Thr Ser Ser Val 50 55 60 Phe Leu Ala Asp Thr Ser Arg Ser Cys Arg Arg Trp Ala Met Val Leu 65 70 75 80 Cys Phe Ser Thr Ser Leu Ser Ser Thr Phe Asn Cys Cys Val Trp Phe 85 90 95 Trp 131 113 PRT Japanese Macaque Herpesvirus 131 Met Gly Thr Gly Leu Arg Gly Ala Leu Tyr Arg Leu Leu Asn Gly Ser 1 5 10 15 Thr Ser Gly Thr His Ser Arg Met Gly Val Arg Ser Pro Met Pro Pro 20 25 30 Arg Ala Trp Pro Arg Arg Trp Ala Cys Arg Gln Lys Asp Ser His Trp 35 40 45 Tyr Val Lys His His Arg Ser Glu His Arg Leu Lys Ser Gly His Pro 50 55 60 Ala Cys Leu Lys Pro Gly Pro Ala Trp Ser Ile Gly Pro Arg Cys Ser 65 70 75 80 Ser Pro Trp Ala Val Arg Thr Arg Thr Ala Gly Ala Arg Trp Ser Phe 85 90 95 Leu Ala Leu Val Leu Asp Arg Ala Asp Gln Arg Trp Ser Gly Val Gly 100 105 110 Ser 132 433 PRT Japanese Macaque Herpesvirus 132 Met Gly Leu Leu Thr Pro Ile Leu Glu Cys Val Pro Asp Val Glu Pro 1 5 10 15 Phe Lys Ser Leu Tyr Asn Ala Pro Arg Lys Pro Val Pro Ile Asn Thr 20 25 30 Leu Pro Ala Ser Leu His Pro His Asp Glu Gln Gln Val Phe Leu Arg 35 40 45 Gln Ala Gln Trp Leu Ser Tyr Arg Phe Ile Pro His Glu Ala Ala Arg 50 55 60 Ser Ser Ser Pro Pro Leu Leu Val Val Ile Asp Pro Glu Asn Leu Val 65 70 75 80 Thr Ala Thr Tyr Ser Ser Gly Gly Pro Ala Asn Phe Glu Ser Arg Pro 85 90 95 Phe Tyr Val Met Pro Gly Pro Tyr Pro Thr Asp Trp Pro Lys Thr Leu 100 105 110 Ser Val Thr Ser Asn Thr Ser Val Thr His Leu Ser His Asp Glu Ile 115 120 125 Cys Asn Leu Phe Thr Thr Leu Ser Arg Glu His Gly Thr Val Gln Gly 130 135 140 Arg Asp Ile Phe Ala Ala Ala Pro Thr Asn Val Thr Pro Glu Arg Thr 145 150 155 160 Ala Asn His Pro Thr Trp Glu Thr Glu Asn Gln Leu Thr Thr Gln Thr 165 170 175 Glu Pro Ala Glu Lys Thr His Val Ile Pro Ala Ser Pro Lys Ala Arg 180 185 190 Thr Asp Pro Ile Ala Glu Thr Thr Ala His His Ser Gln Gly Gln Ala 195 200 205 Ser Gln His Ala Asn Asn Val Asn Gln Pro Gly Gln Ile Thr Ser His 210 215 220 Ala Ser Arg Asn Lys Pro Ser Thr Ala Pro Gln Ala Ser Ser Arg Pro 225 230 235 240 Glu Lys Leu Asn Thr Gln Thr Val Pro Arg Leu Ile Ser Gln Thr Ser 245 250 255 Glu Thr Ala His Ile Asn His Pro Ala Ser Gly Gln Val Thr Glu Pro 260 265 270 Lys Gly Ile Phe Gly Thr Tyr Lys Pro Arg Val Leu Thr Glu Pro Ala 275 280 285 Lys Pro Ala His Ala Ser Ile Ala Ser Arg Gln Pro Glu Ala Thr Thr 290 295 300 Thr Val Pro Lys Leu Pro Ile Asn Ala Pro Thr Ala Lys Val Phe Ile 305 310 315 320 Gly Thr Ala Ser Lys Phe Leu Pro Asp Val Glu Glu Ser His Gly Thr 325 330 335 Thr Pro Gly Ala His Gln Ser Lys Ile Asp Gln Lys Gln Tyr Gly Glu 340 345 350 Ser Gln Pro His Arg Thr Pro His Leu Glu Glu Val Pro Arg Ala Pro 355 360 365 His Val Asp Thr Pro Thr Ser Ala His Ile Asn Val Pro Ser Ser Gln 370 375 380 Gly Pro Lys Thr Ile His Ala Arg Val Thr Pro Gly Ile Gln Thr Val 385 390 395 400 Thr Pro Ser Ala Pro Pro Pro Ala Gly Gln Ile Arg Ala Phe Asn Thr 405 410 415 Arg Phe Pro Glu Pro Thr Ala Gly Arg Ser Thr Thr Asn Arg Met Trp 420 425 430 Asn 133 140 PRT Japanese Macaque Herpesvirus 133 Met Leu Tyr Phe Gln Glu Phe Gly Gly Val Leu Val Asp Glu Ser Leu 1 5 10 15 Arg Leu Asp Arg Met Gly Arg Ser Ile Tyr Ser Arg Pro Val Arg Ala 20 25 30 Cys Glu Thr His Phe Val Phe Trp Ala Ile Leu Leu Pro His Trp Leu 35 40 45 Gly Ser Ile Pro His Pro Ile Arg Arg Gly Ala Thr Gly Arg Arg Phe 50 55 60 Trp Glu Ala Cys Ile Glu Cys Ala Asp Leu Thr Gly Arg Trp Gly Gly 65 70 75 80 Ala Gly Ser Tyr Cys Leu Asn Thr Gly Cys Tyr Ala Arg Val Tyr Cys 85 90 95 Phe Trp Thr Leu Ala Arg Gly Asp Val Tyr Val Cys Ala Gly Trp Ser 100 105 110 Val Asp Val Arg Arg Pro Trp Asn Leu Phe Lys Val Trp Gly Ala Val 115 120 125 Arg Leu Thr Phe Ala Val Leu Phe Leu Ile Tyr Leu 130 135 140 134 169 PRT Japanese Macaque Herpesvirus 134 Met Ser Ser Leu Arg Val Lys Glu Pro Ile Val Gln Gly Arg Leu Glu 1 5 10 15 His Asp Tyr Pro Asn His Pro Leu Val Ala Glu Met Asn Asn Leu Pro 20 25 30 Gln Gly Asp Met Ser Pro Ala Gln Tyr Ala Ile Ala Lys Arg Asn Tyr 35 40 45 Leu Val Phe Leu Thr Ala Lys His His Tyr Asp Met Tyr Thr Gln Lys 50 55 60 Lys Asn Gly Ile Leu Arg Lys Asp His Leu Arg Gly Leu Arg Gly Lys 65 70 75 80 Lys Asp Ala Ser Ser Ser Ile Ser Ser Val Leu Ser Gly Ser Gly Ser 85 90 95 Ala Ala Pro Ser Val Ala Pro Val Ala Ser Thr Leu Gly Ser Asn Ser 100 105 110 Phe Thr Thr Ile Ser Ser Gly Pro His Ser Leu Ile Gly Ser Ile Gly 115 120 125 Pro Thr Pro Gly Gly Gly Gly Pro Gly Ser Val Ala Ser Ser Gly Ile 130 135 140 Gly Ser Thr Ser Leu Ser Pro Ser Asp Ala Thr Thr Leu Asp Thr Arg 145 150 155 160 Arg Ser Ser Gln Asn Lys Lys Ser Lys 165 135 86 PRT Japanese Macaque Herpesvirus 135 Met Pro Glu Asp Ala Thr Leu Pro Gly Pro Pro Pro Pro Gly Val Gly 1 5 10 15 Pro Ile Glu Pro Ile Asn Glu Trp Gly Pro Leu Glu Ile Val Val Lys 20 25 30 Leu Phe Asp Pro Arg Val Glu Ala Thr Gly Ala Thr Leu Gly Ala Ala 35 40 45 Glu Pro Asp Pro Asp Lys Thr Leu Glu Ile Leu Glu Leu Ala Ser Phe 50 55 60 Leu Pro Arg Arg Pro Arg Arg Trp Ser Leu Arg Lys Ile Pro Phe Phe 65 70 75 80 Phe Cys Val Tyr Met Ser 85 136 448 PRT Japanese Macaque Herpesvirus 136 Met Ala Ser Gly Arg Leu Pro Asp Leu Ala Glu Asp Glu Ala Ala Cys 1 5 10 15 His Gly Arg Val Pro Tyr Pro Val His His Trp Leu Asp Cys Ser Arg 20 25 30 Leu Gly Leu Asp Phe Ala Ala Ser Met Arg Ala Ile Gly Leu Cys Pro 35 40 45 Glu Cys Tyr Val Cys Phe Val Thr Tyr Gly Leu Gly Ala Trp Glu Gly 50 55 60 Gln Pro Pro Glu Trp Ala Arg Thr Leu Ile Ser Ala Pro Ser Phe Gln 65 70 75 80 Thr Ala Leu Asn Asp Ile Ala Thr Gly Trp Met Pro Asp Asn Pro Pro 85 90 95 Lys Asn Gly Asp Val Lys Ser Arg Leu His Asp Thr Gly Arg Leu Leu 100 105 110 Leu Glu Ala Tyr Ala Trp Val Leu Arg Cys Ile Cys Thr Gly Val Gly 115 120 125 Tyr Ala Asp Asn Glu Gly Leu Ser Leu Thr Ala Val Pro Arg Gly Ala 130 135 140 Trp Ser Arg Tyr Leu Val Val Ser Phe Pro Arg Ala Cys Cys Phe Val 145 150 155 160 Cys Lys Thr Leu Asn Cys Arg Gln Arg Phe Pro Leu Val Thr Cys Ser 165 170 175 Pro Gln His Ala Leu Asp Leu Pro Val Leu Arg Lys Lys Trp Asn Gly 180 185 190 Ala Gly Cys Val Ala Met Gln Leu Asn Val Pro Ser Ile Ser Arg Arg 195 200 205 Leu Gly Ala Asn Leu Asp Glu Arg Gly Leu Gly Pro Ser Asp Ala Gly 210 215 220 Leu Leu Ala Ser Leu Arg Glu Leu Ala Pro Thr Val Pro Cys Gly Asn 225 230 235 240 Pro Phe Asn Ala Leu Leu Arg Ser Leu Thr Phe Arg Gly Leu Leu Ser 245 250 255 Met Ser Arg Val Val Leu Pro Ile Gly Glu Ser Thr Glu Thr Glu Ile 260 265 270 Ser Arg Asp Leu Gly Gln Lys Val Leu Ala Tyr Asn Val Leu Phe Pro 275 280 285 Cys Ile Ser Leu Pro Val Trp Ser Gln Val Val Ala Arg Ser Val Leu 290 295 300 Glu Lys Thr Val Pro Ala Pro Arg Val Val Val Cys Leu Glu Cys Gly 305 310 315 320 Tyr Cys Leu Asn Phe Gly Arg Gly Lys Phe Glu Thr Val Asn Phe Pro 325 330 335 Pro Thr Asn Val Phe Phe Ser Arg Asp Gln Lys Glu Lys Gln Leu Ser 340 345 350 Ile Cys Ala Thr Thr Gly Arg Val Tyr Cys Ser Tyr Cys Gly Gly Ser 355 360 365 His Met Arg Val Ile Ser Leu Phe Glu Ile Thr Cys Val Gly Asp Pro 370 375 380 Tyr Leu Arg Cys Val Leu Ala Asn Asn Ala Ala His Ser Ile Arg Asp 385 390 395 400 Ala Asn Ser Leu Val Ser Val Val Val Pro Cys Leu Ala Ser Pro Asp 405 410 415 Cys Ala Thr Gly Leu Leu Lys His Leu Arg Val Ala Glu Leu Phe Tyr 420 425 430 Leu Thr Ser Ser Ile Ser Ser Leu Ser Cys Gly Lys Cys Asn Arg Ser 435 440 445 137 135 PRT Japanese Macaque Herpesvirus 137 Met Gly Ser Thr Thr Arg Asp Met Leu Asn Arg Pro Leu Asn Val Arg 1 5 10 15 Leu Leu Arg Arg Ala Leu Asn Gly Leu Pro His Gly Thr Val Gly Ala 20 25 30 Ser Ser Arg Ser Glu Ala Ser Ser Pro Ala Ser Glu Gly Pro Arg Pro 35 40 45 Arg Ser Ser Arg Leu Ala Pro Lys Arg Leu Glu Met Asp Gly Thr Phe 50 55 60 Ser Cys Ile Ala Thr Gln Pro Ala Pro Phe His Phe Phe Arg Lys Thr 65 70 75 80 Gly Lys Ser Ser Ala Cys Cys Gly Glu His Val Thr Arg Gly Asn Arg 85 90 95 Trp Arg Gln Leu Arg Val Leu His Thr Lys Gln His Ala Leu Gly Asn 100 105 110 Asp Thr Thr Arg Tyr Leu Asp His Ala Pro Leu Gly Thr Ala Val Lys 115 120 125 Leu Arg Pro Ser Leu Ser Ala 130 135 138 268 PRT Japanese Macaque Herpesvirus 138 Met Ser Ser Gly Lys Arg Leu Val Asp Glu Leu Cys Asp Val Val Val 1 5 10 15 Ser Tyr Leu Gly Pro Ser Gly Ile Ser Leu Asp Leu Glu Arg Cys Gln 20 25 30 Asp Gly Ala Pro Val Tyr Ala Lys Gly Gly Ala Val Pro Val Cys Thr 35 40 45 Val Arg Leu Gln His Gly Cys Val Tyr His Leu Glu Phe Val Tyr Lys 50 55 60 Phe Trp Leu His Lys Leu Glu Arg Leu Ala Tyr Pro Phe Ala Pro Cys 65 70 75 80 Phe Val Ile Thr Asn Asn Gly Leu Ala Thr Thr Leu Lys Cys Phe Leu 85 90 95 Cys Lys Pro Arg Asp Ala Asp Ala Gln Phe Gly Lys Asn Leu Pro Ile 100 105 110 Asn Ser Asp Val Tyr Leu Glu Arg Asn Ser Ser Val Phe Leu Gly Gln 115 120 125 Asp Asp Phe Met Lys Phe Lys Ala Arg Leu Val Phe Ser Gly Asp Leu 130 135 140 Asn Val Tyr Ser Ser Met Val Ile Cys Arg Thr Tyr Phe Thr Glu His 145 150 155 160 Arg Gln Val Leu Gln Phe Leu Val Val Thr Pro Lys Ser Ala Lys Arg 165 170 175 Leu Lys Thr Leu Leu Arg Thr Val Phe Ala Leu Thr Gly His Ser Asp 180 185 190 Gly Leu Gly Ala Leu Arg Arg Thr Gly Ser Val Ala Arg Pro Ser Gly 195 200 205 Ser Glu Leu Thr Asp Ile Gly Ser Gly Glu Arg Cys Gly Asn Asp Arg 210 215 220 Leu Thr Asp Ser Ile Gly Thr Ile Gly Gly Trp Pro Arg Gly Ala Cys 225 230 235 240 Leu Thr Trp Leu Lys Thr Lys Leu Pro Val Met Gly Ala Phe Leu Ile 245 250 255 Leu Ser Ile Ile Gly Trp Ile Val Leu Gly Trp Ala 260 265 139 104 PRT Japanese Macaque Herpesvirus 139 Met Met Asp Arg Ile Arg Asn Ala Pro Met Thr Gly Ser Phe Val Phe 1 5 10 15 Ser Gln Val Arg Gln Ala Pro Arg Gly His Pro Pro Ile Val Pro Met 20 25 30 Glu Ser Val Asn Arg Ser Leu Pro His Arg Ser Pro Leu Pro Ile Ser 35 40 45 Val Asn Ser Asp Pro Glu Gly Arg Ala Thr Glu Pro Val Arg Leu Asn 50 55 60 Ala Pro Arg Pro Ser Glu Cys Pro Val Arg Ala Lys Thr Val Leu Arg 65 70 75 80 Arg Val Phe Asn Arg Leu Ala Leu Phe Gly Val Thr Thr Lys Asn Cys 85 90 95 Lys Thr Cys Arg Cys Ser Val Lys 100 140 86 PRT Japanese Macaque Herpesvirus 140 Met Ser Gly Asp Asp Leu Leu Ala Phe Glu Ser Leu Leu Pro Glu Asp 1 5 10 15 Met Lys Ile Met Phe Pro Thr Ile Tyr Ser Arg Leu Asn Ala Ile Asn 20 25 30 Tyr Cys Gln Tyr Leu Lys Thr Phe Leu Cys Asn Arg Ala Gln Thr Arg 35 40 45 Ser Ala His Cys Glu His Cys Met Val Leu Asp Ala Lys Val Asn Ala 50 55 60 Val Lys Gln Val Ile His Lys Ile Val Ser Thr Asp Ala Val Phe Thr 65 70 75 80 Gly Ala Ala His Ser Thr 85 141 457 PRT Japanese Macaque Herpesvirus 141 Met Phe Val Pro Trp Gln Leu Glu Thr Leu Met Lys His Trp Pro Ser 1 5 10 15 Leu Arg Glu Leu Val Glu Gln Ser Phe Leu Pro Gly Thr Pro Asp Val 20 25 30 Ala Phe Asn Ser Pro Val Leu Ile His Thr Gln Asp Ser Leu Gln Pro 35 40 45 Ala Ser Ser Cys Arg Val Cys Asn Ile Leu Phe Thr Leu Val Arg Thr 50 55 60 Phe Pro Pro Pro Asp Ser Phe Phe Glu Asp Tyr Gly Trp Leu Cys Leu 65 70 75 80 Thr Cys Leu Tyr Ala Pro Arg Ser Trp Thr Ala Thr Leu Met Val Ala 85 90 95 Ala Asp Leu Leu Glu Leu Ile His Met Tyr Phe Pro Gln Arg Val Lys 100 105 110 Asp Gly Pro Val Tyr Thr Thr Gln Asn Ile Leu Gly Ile Asp Val Gln 115 120 125 Leu His Phe Phe Ala Thr Arg Cys Phe Arg Pro Ile Asp Arg Glu Gln 130 135 140 Ile Leu His Thr Ser His Leu Asn Phe Leu Gln Thr Glu Phe Ile Arg 145 150 155 160 Gly Met Leu Glu Gly Thr Ile Pro Gly Ser Phe Cys Phe Lys Thr Ser 165 170 175 Trp Pro Arg Thr Glu Lys Asp Asp Gln Gln Pro Thr Val Ala Cys Cys 180 185 190 Ser Val Gly Arg Gly Asn His Ala Asn Arg Asp Asn His Leu Pro Asp 195 200 205 Asp Leu Glu Glu Ala Phe Asn Ser Thr Asn Ala Lys Glu Lys Pro Ser 210 215 220 Ile Leu Gly Val Phe Ser Ala Thr Trp Ser Glu Ser Gln Leu Leu Gly 225 230 235 240 Ser Asp Thr Gln Gln Ala Thr Ile His Ser Gln Pro Ser Thr Phe Pro 245 250 255 Thr Pro Glu Asp Ala Asp Gln Ser Gln Gly Pro Cys Leu Met His Pro 260 265 270 Thr Leu Asn Leu Lys Thr Lys Asn His Thr Ala Ser Ile Cys Val Leu 275 280 285 Cys Glu Cys Leu Ala Ala His Pro Asp Ala Gly Pro Val Leu Arg Asp 290 295 300 Leu Arg Arg Asp Ile Leu Glu Asn Met Glu Asn Asn Val Lys Leu Val 305 310 315 320 Asn Arg Ile Ser Tyr Ile Leu Asn Asp Pro Asp Ser Leu Ser His Val 325 330 335 Arg Asp Glu His Leu Arg Gly Leu Ile Lys Arg Cys Ser Ala Gln Glu 340 345 350 Ile His Lys His Phe Phe Cys Asp Pro Leu Cys Val Leu Asn Thr Tyr 355 360 365 Ser His Cys Pro Ala Val Leu Phe Lys Cys Pro Pro Pro Glu Lys Tyr 370 375 380 Lys Lys Leu Lys Ala Arg Leu Ala Thr Gly Glu Phe Leu Asp Cys Asn 385 390 395 400 Arg Ile Phe Asp Cys Glu Thr Leu Gln Thr Leu Ala Val Leu Phe Lys 405 410 415 Gly Ser Gln Leu Ala Lys Ile Gly Lys Thr Thr Ser Leu Glu Ile Ile 420 425 430 Arg Glu Leu Gly Phe Gln Leu Arg Arg His Asn Ile Gln Ile Thr His 435 440 445 Pro Phe Gln Thr Ser Asn Leu Tyr Ile 450 455 142 127 PRT Japanese Macaque Herpesvirus 142 Met Tyr Asp Met Arg Leu Thr Ser Leu Thr Leu Phe Ser Met Phe Ser 1 5 10 15 Arg Met Ser Arg Arg Arg Ser Leu Arg Thr Gly Pro Ala Ser Gly Trp 20 25 30 Ala Ala Arg His Ser His Arg Thr Gln Met Asp Ala Val Trp Phe Phe 35 40 45 Val Leu Arg Leu Ser Val Gly Cys Ile Arg Gln Gly Pro Cys Asp Trp 50 55 60 Ser Ala Ser Ser Gly Val Gly Lys Val Glu Gly Cys Glu Trp Ile Val 65 70 75 80 Ala Cys Cys Val Ser Glu Pro Arg Ser Trp Asp Ser Asp His Val Ala 85 90 95 Glu Lys Thr Pro Arg Met Leu Gly Phe Ser Leu Ala Phe Val Glu Leu 100 105 110 Asn Ala Ser Ser Arg Ser Ser Gly Arg Trp Leu Ser Arg Leu Ala 115 120 125 143 108 PRT Japanese Macaque Herpesvirus 143 Met Phe Asp Glu Cys Pro Asn Asp Glu Arg Asp Thr His Arg Pro Gly 1 5 10 15 Ala Met Val Phe Arg Phe Asn Gly Asn Ile Thr Asp Phe Glu Val His 20 25 30 Ile Gly Val Pro Ile Ser Leu Lys Lys Ser Thr Pro Ser Ser Trp Arg 35 40 45 Arg Val Arg Ala Glu Lys Asn Cys Val Ser Glu Thr Asn Phe Phe His 50 55 60 Cys Ile Ile Ser Leu Leu Gln Leu Pro Cys Leu Asp Ala Gly Cys Val 65 70 75 80 Asp Trp Gly Pro Ser Gly Arg Leu Thr Leu Gly Ala Tyr Gly Val Arg 85 90 95 Asp Ala Asn Arg Arg Leu Gly Cys Phe Gly Ile Val 100 105 144 297 PRT Japanese Macaque Herpesvirus 144 Met Pro Lys Gln Pro Arg Arg Arg Leu Ala Ser Arg Thr Pro Tyr Ala 1 5 10 15 Pro Ser Val Lys Arg Pro Asp Gly Pro Gln Ser Thr Gln Pro Ala Ser 20 25 30 Arg His Gly Ser Cys Lys Ser Glu Ile Met Gln Trp Lys Lys Leu Val 35 40 45 Ser Asp Thr Gln Phe Phe Ser Ala Leu Thr Arg Arg His Glu Leu Gly 50 55 60 Val Asp Phe Leu Arg Glu Met Gly Thr Pro Ile Cys Thr Ser Lys Ser 65 70 75 80 Val Met Leu Pro Leu Asn Leu Lys Thr Ile Ala Pro Gly Arg Cys Val 85 90 95 Ser Leu Ser Ser Phe Gly His Ser Ser Asn Met Gly Phe Asn Cys Ser 100 105 110 Ser Cys Thr Pro Thr Asp Arg Ser Ala Val Ser Leu Asp Ala Asn Ala 115 120 125 Leu Gly Glu Asp Ser Ala Arg Lys Asn Ser Glu Leu Cys Ser Val Ala 130 135 140 Leu Thr Phe Tyr His His Ala Glu Lys Val Val Gln His Lys Gly Phe 145 150 155 160 Tyr Leu Ser Leu Leu Ser His Ser Met Glu Val Val Arg Arg Ser Phe 165 170 175 Thr Gln Pro Gly Leu Leu Tyr Ala His Leu Val Leu Lys Thr Phe Gly 180 185 190 His Asp Pro Leu Pro Ile Phe Thr Val Asp Ala Asn Glu Arg Leu Ala 195 200 205 Leu Trp Ala Val Phe His Thr Arg Asp Leu His Leu Gly Glu Thr Ser 210 215 220 Leu Arg Leu Ile Met Asp Asn Leu Pro Asn Tyr Asp Ile Thr Val Asp 225 230 235 240 Cys Ile Lys Gln Thr Tyr Ile Met Lys Phe Thr Pro Ser Arg Pro Asp 245 250 255 Asn Ala Thr Val Thr Val Pro Val Asn Ser Ile Cys Glu Ala Val Ala 260 265 270 Thr Leu Asp Cys Thr Asp Glu Phe Arg Glu Glu Ile Gln Arg Gly Thr 275 280 285 Thr Ile Ile Asn Ser Gln Gly Ser Leu 290 295 145 83 PRT Japanese Macaque Herpesvirus 145 Met Leu Thr Arg Ala Pro Arg Leu Gly Ala Ser Val Gln Leu Thr Ala 1 5 10 15 Val Arg Leu Leu Leu Leu Phe Leu Thr Ser Ser Thr Pro Thr Ala Ile 20 25 30 Asn Cys Thr Lys Pro Gly Ser Val Phe Phe Trp Leu Ser Trp Pro Lys 35 40 45 Val Phe Met Glu Asn His Tyr Ser Phe Ile Ser Val Asn Ser Val Ser 50 55 60 Ile Thr Val Val Ala Ala Gly Lys Ile Ser Ser Arg Gly Lys Thr Ala 65 70 75 80 Thr Asn Cys 146 289 PRT Japanese Macaque Herpesvirus 146 Met Trp Cys Leu Val Gln Arg Ala Gly Pro Pro Val Gly Cys Arg Ser 1 5 10 15 Pro Gly Gly Val Gln Val Pro Arg Trp Gly Ala Gly Pro Pro Val Gly 20 25 30 Cys Arg Ser Pro Gly Gly Val Gln Val Pro Arg Trp Gly Ala Gly Pro 35 40 45 Pro Val Gly Cys Arg Ser Pro Gly Gly Val Gln Val Pro Arg Trp Gly 50 55 60 Ala Gly Pro Pro Val Gly Cys Arg Ser Pro Gly Gly Val Gln Val Pro 65 70 75 80 Arg Trp Gly Ala Gly Pro Pro Val Gly Cys Arg Ser Pro Gly Gly Val 85 90 95 Gln Val Pro Arg Trp Gly Ala Gly Pro Pro Val Gly Cys Arg Ser Pro 100 105 110 Gly Gly Val Gln Val Pro Arg Trp Gly Ala Gly Pro Pro Val Gly Cys 115 120 125 Arg Ser Pro Gly Gly Val Gln Val Pro Arg Trp Gly Ala Gly Pro Pro 130 135 140 Val Gly Cys Arg Ser Pro Gly Gly Val Gln Val Pro Arg Trp Gly Ala 145 150 155 160 Gly Pro Pro Val Gly Cys Arg Ser Pro Gly Gly Val Gln Val Pro Arg 165 170 175 Trp Gly Ala Gly Pro Pro Val Gly Cys Arg Ser Pro Gly Gly Val Gln 180 185 190 Val Pro Arg Trp Gly Ala Gly Pro Pro Val Gly Cys Arg Ser Pro Gly 195 200 205 Gly Ala Pro Gly Gly Ser Gly Trp Gly Gly Gly Ser Gly Trp Leu Arg 210 215 220 Val Gly Trp Arg Leu Arg Val Ala Pro Gly Gly Val Ala Ala Pro Gly 225 230 235 240 Gly Ser Gly Trp Ala Gln Val Leu Lys Ala Thr Val Asn Pro Thr Ala 245 250 255 Asn Pro Thr Gln Lys Ser Pro Cys Ala Ser Arg Ala Glu Ala Arg Leu 260 265 270 Leu Thr Cys Ala Ser Gly Ala Leu Tyr Ile Gly Gln Asn Thr Leu Pro 275 280 285 Lys 147 108 PRT Japanese Macaque Herpesvirus 147 Met Gly Asn Pro Arg Ile Asp Arg Ser His Ser Lys His Val Gly Phe 1 5 10 15 Thr Leu Phe Gly Glu Ser Pro Leu Ala Gly Pro Asn Val Pro Ala Arg 20 25 30 Cys Thr Trp Val Leu Arg Asn Ala Lys Leu Pro Leu Pro Cys Arg Val 35 40 45 Pro Tyr Ser Cys Ser Ala Ile Phe Glu Tyr Thr Ala Leu His Gly Trp 50 55 60 Arg Ala Val Gly Arg Trp Cys Ala Asn Gln Lys Leu Met Ile His Leu 65 70 75 80 Leu Val Leu Trp Leu His Asn Asn Thr Met Leu Leu Ile Leu Gly Gly 85 90 95 Cys Phe Gly Leu Tyr Lys Gly Arg Arg Lys His Arg 100 105 148 234 PRT Japanese Macaque Herpesvirus 148 Met Tyr Ser Trp Gly Glu Phe Arg Thr Met Glu Arg Lys Met Ser Leu 1 5 10 15 Arg Val Thr Arg Gly Ser Gln Lys His Ile Thr Met Gly Leu Phe Gly 20 25 30 Ala His Lys Arg Ala Val Gly Asn Gly Leu Gly Gly Ala Pro Ala Pro 35 40 45 Pro Cys Ala Arg Asn Leu Gly Arg Gly Val Arg Arg Gly Ser Pro Lys 50 55 60 His Val Leu Met Val Ala Ala Arg Thr His Arg Pro Leu Phe Gly Ala 65 70 75 80 Gly Val Ile Arg Arg Ser Ala Gln Asn Val Ala His Gly Thr His Cys 85 90 95 Thr His Gly Ala His Glu Gly Gly Gly Val Ala Gly Arg Ser His Arg 100 105 110 Ala Gly Arg Gly Ala Arg Arg Leu Trp His Arg Ala Ser Asp Val Tyr 115 120 125 Gly Arg Asn Pro Leu Ser Arg Gly Ile Lys Gly Arg Arg Gln Gly Arg 130 135 140 Phe Pro Leu Ala Arg Arg Ala Val Asn Gln Thr Asp Ala Arg Arg Arg 145 150 155 160 Leu Val Val Ala Thr Val Gly Phe Leu Leu Arg Cys Arg Val Pro Ser 165 170 175 Arg Asp Trp Leu Gly Asp Leu Ser Ile Lys Asn Ala Arg Arg Pro Leu 180 185 190 Ala Gln Pro Pro Val Asn His Gly Ile Leu Ala Ala Asn Trp Pro Lys 195 200 205 Gln Thr Ala Asn Pro Arg Val Gly Phe Cys Leu Gln Val Pro Leu Tyr 210 215 220 Tyr Ile Tyr Ser Ile Ile Phe Phe Pro Cys 225 230 149 85 PRT Japanese Macaque Herpesvirus 149 Met Thr Pro Ala Pro Lys Ser Gly Arg Trp Val Arg Ala Ala Thr Ile 1 5 10 15 Lys Thr Cys Phe Gly Asp Pro Arg Leu Thr Pro Arg Pro Lys Leu Arg 20 25 30 Ala His Gly Gly Ala Gly Ala Pro Pro Ser Pro Phe Pro Thr Ala Arg 35 40 45 Leu Trp Ala Pro Asn Arg Pro Met Val Ile Cys Phe Cys Asp Pro Arg 50 55 60 Val Thr Arg Ser Asp Ile Leu Arg Ser Met Val Leu Asn Ser Pro His 65 70 75 80 Glu Tyr Met Phe Arg 85 150 88 PRT Japanese Macaque Herpesvirus 150 Met Val Pro Phe Gly Ala His Gly Ala Val Phe Ala Ala Arg Gly Arg 1 5 10 15 Arg Arg Val Thr Glu Thr Cys Thr His Gly Ala Asn Ser Gly Pro Trp 20 25 30 Ser Ala Lys Cys Arg Ser Gly Ser Pro Glu Gly His Arg Asn Ile Ser 35 40 45 Pro Trp Ala Tyr Leu Val Pro Ile Ser Gly Pro Trp Glu Met Gly Ser 50 55 60 Val Gly Arg Arg Arg His His Val Pro Ala Ile Trp Gly Ala Gly Ser 65 70 75 80 Gly Gly Gly His Arg Asn Met Phe 85 151 94 PRT Japanese Macaque Herpesvirus 151 Met Ser Cys Glu His Phe Pro Pro Gly Tyr Asn Gly Gln Glu Ser Ala 1 5 10 15 Gly Lys Thr Ser Thr Gly Leu Pro Val Gly Glu Arg Glu Ala Arg Arg 20 25 30 Tyr Ala Ala Cys Val Ser Glu Val Ala Pro Met Gly Arg Met Thr Thr 35 40 45 Pro Ala Thr Arg Arg Ala Ala Gly Ala Asp Ile Ser Gln Asn Arg Pro 50 55 60 Arg Arg Gln Ala Ala Arg Leu Pro Pro Pro Thr Thr Leu Ile Leu Ala 65 70 75 80 Phe Lys Leu Leu Phe Lys Ala Arg Leu Phe Val Ala Arg Ala 85 90 152 174 PRT Japanese Macaque Herpesvirus 152 Met Phe Pro His Lys Arg Ile Val Asp Leu Gly Arg His Leu Glu Ala 1 5 10 15 Asp Asp Arg Glu Ala Val Leu Trp Leu Phe Asp Arg Pro Val Ser Asp 20 25 30 Asn Thr Pro Glu Gly Phe Ala Asn Gly Leu Cys Pro Pro Thr Gly Glu 35 40 45 Pro Gly Ile Pro Phe Pro Val Leu Leu Glu Ala Val Phe Leu Val Gly 50 55 60 Arg Leu Asp Leu Val Ser Thr Phe Phe Leu Leu Asp Val Gly Phe Ile 65 70 75 80 Val Glu Arg Leu Arg Ser Ser Pro Ser Tyr Phe Ser Pro Tyr Lys His 85 90 95 Leu Met Leu Ser Ile Asn Arg Gln Leu Ser Glu Arg Asp Val Lys Asn 100 105 110 Leu Val Phe Leu Thr Gly Asn Gln Leu Gly Arg Lys Arg Asn Gln Ser 115 120 125 Pro Thr Phe Phe Gln Trp Ile Ser Gln Met Glu Lys Ala Ala Leu Val 130 135 140 Ser Pro Ser Asp Tyr Leu Val Leu Lys Asp Leu Leu Gln Ala Val Ser 145 150 155 160 Arg Arg Asp Val Ala Lys Val Val Ala Ala Asn Ala Pro Gly 165 170 153 254 PRT Japanese Macaque Herpesvirus 153 Met Ala Phe Val Gly Pro Val Pro Thr Gly Thr Ile Asp Pro Val Leu 1 5 10 15 Tyr Gln Asp Arg Ala Leu Ser Asn Leu Leu Ala His Glu Thr Ser Phe 20 25 30 Val Thr Ser Thr Ala Cys Tyr Gly Thr Val Gln Thr Glu Val Thr Leu 35 40 45 Gly Met Arg Val Ile Leu Gly Thr Trp Met Arg Ser Val Ala Arg Ala 50 55 60 His Gln Ala Asp Ala Ser Val Phe Pro Leu Ala Val Ser Ile Leu Asp 65 70 75 80 Arg Tyr Leu Glu Cys Arg Ser Ile Pro Arg Arg Arg Phe Gln Arg Leu 85 90 95 Gly Ala Ala Cys Leu Phe Leu Ala Gly Lys Ile Arg Asp Leu Asn Pro 100 105 110 Phe Lys Ala Ala Phe Leu Cys Phe Cys Ala Ala Asp Asp Phe Ser Val 115 120 125 Ala Asp Leu Leu Lys Gln Glu Lys Ser Val Leu Lys Ala Leu Arg Trp 130 135 140 Lys Leu Glu Ala Val Leu Pro Thr Asp Ala Ile Gly Pro Ala Leu Phe 145 150 155 160 Lys Ser Gly Phe Thr Lys Glu Gln Leu Phe Ala Leu His Ser Arg Val 165 170 175 Val Glu Ser Val His Lys Ala Ile Val Asn Pro Val Thr Gly Gly Leu 180 185 190 Ser Pro Ser Leu Val Ala Ala Ala Cys Ala Leu Phe Ser Leu Gly Ala 195 200 205 Ala Ala Pro Pro Leu Asp Lys Leu Ala Glu Ala Ile Gly Val Ser Ala 210 215 220 Ala Thr Leu Thr Ala Ala Ala Glu Ser Val Ala Thr Thr Leu Arg Glu 225 230 235 240 Leu Asp Glu Asp Arg Ile Leu Asn Asn Ala Arg Gly Ser Ser 245 250 154 436 PRT Japanese Macaque Herpesvirus 154 Met Trp Gly Ser Arg Gln His Arg Ser Gly Ile Val Ser Gly His Gly 1 5 10 15 Leu Arg Ser Ser Cys Arg Gly His Cys Gly Arg Arg Gly Gly Thr Arg 20 25 30 Glu Gln Ala Gly Gly Arg Ser Arg Gly Arg Gly Arg Gly Ala Ala Ala 35 40 45 Pro Ala Ser Ala Ser Ala Ala Ser Ala Ser Pro Thr Pro Pro Gly Pro 50 55 60 Gln Val Leu Val Val Val Glu Gln Gly His Gly Ser Asp Thr Glu Thr 65 70 75 80 Ala Thr Glu Ser Gly His Gly Ser Ser Gln Gly Ser Pro Ser Gly Ser 85 90 95 Gly Ser Glu Ser Val Ile Val Leu Gly Ser Pro Thr Pro Ser Pro Ser 100 105 110 Gly Ser Ala Pro Val Leu Ala Ser Asp Leu Ser Pro Arg Asn Thr Ser 115 120 125 Gly Ser Ser Pro Gly Ser Pro Ala Ser His Ser Pro Pro Pro Ser Pro 130 135 140 Pro Ser His Pro Ala Pro Leu Ser Pro Ala Pro Pro Ser Ser His His 145 150 155 160 Pro Ser Pro Asp Pro Gln Pro Pro Ser Phe Leu Gln Pro Leu Pro His 165 170 175 Asp Ser Pro Glu Pro Pro Gly Pro Pro Thr Ser Ser Pro Pro Pro Asn 180 185 190 Ser Pro Gly Pro Pro Gln Ser Pro Thr Pro Thr Ser Ser Pro Pro Pro 195 200 205 Gln Ser Pro Pro Asp Ser Pro Gly Pro Gln Gln Ser Pro Thr Pro Gln 210 215 220 Gln Ala Pro Ser Pro Asn Thr Gln Gln Ala Val Ser His Thr Asp His 225 230 235 240 Pro Ala Gly Pro Ser Arg Pro Gly Pro Pro Phe Pro Gly His Thr Ser 245 250 255 His Thr Tyr Thr Val Gly Gly Trp Gly Pro Pro Arg Arg Pro Gly Gly 260 265 270 Val Pro Cys Leu Arg Leu Arg Cys Thr Ser His Asn Ser His Glu Asp 275 280 285 Glu Val Pro Glu Arg Gln Arg Glu Gln Glu Gly Glu Glu Arg Gln Gln 290 295 300 Gln Pro Ala Arg Pro Pro Arg Pro Pro Arg Tyr Pro Ile Pro Ile Pro 305 310 315 320 Tyr Pro His Pro Arg Arg Arg Tyr Gln Glu Asn Thr Ala His Lys Glu 325 330 335 Asp Phe Ile Val Arg Arg Trp Glu Thr Gly Ser Thr Pro Leu Asp Arg 340 345 350 Ala Arg Gly Val Thr Glu Ser Ser Phe Val Thr Gln Thr Pro Ile His 355 360 365 Cys Ile Ala Trp Gln Gly Ala Tyr Ser Phe Pro Gly Leu Glu His Pro 370 375 380 Ala Ser Ala Phe Cys Arg Thr His Leu Glu Val Pro Ser Ser Arg Leu 385 390 395 400 Phe Ala Ser Arg Cys Ser Val Lys Val Ala Glu Pro Pro Arg Pro Ser 405 410 415 Lys Lys Pro Val Ala Gly Gly Asn Asn Phe Thr His Pro Pro Pro Thr 420 425 430 Ser Met Leu Ala 435 155 126 PRT Japanese Macaque Herpesvirus 155 Met Gly Pro Val Glu Ala Leu Ala Ile Ala Val Val Gln Val Ser Arg 1 5 10 15 Ala Gly Ile Ala Glu Gly Ala Arg Thr Leu Ala Leu Ala Ile Val Val 20 25 30 Val Gln Val Ser Trp Glu Gly Ala Arg Thr Leu Glu Ala Gln Ala Val 35 40 45 Gln Val Ser Arg Gly Ala Thr Val Ala Lys Thr Thr Glu Ala Ala Asp 50 55 60 Arg Ala Met Asp Asp Ala Thr Thr Ala Val Gln Val Arg Gly Gly Arg 65 70 75 80 Gly Ala Met Gly Val Met Val Gly Ala Asn Ala Met Arg Gly Ile Pro 85 90 95 Gly Thr Thr Leu Met Cys Phe Glu Val Thr Gly Leu Lys Leu Thr Pro 100 105 110 Ala Gln Thr Arg Leu Ala Met Ala Leu Glu Ile Pro Thr Arg 115 120 125 156 108 PRT Japanese Macaque Herpesvirus 156 Met Thr Asp Ser Asp Pro Asp Pro Glu Gly Asp Pro Cys Asp Asp Pro 1 5 10 15 Cys Pro Asp Ser Val Ala Val Ser Val Ser Asp Pro Cys Pro Cys Ser 20 25 30 Thr Thr Thr Arg Thr Cys Gly Pro Gly Gly Val Gly Glu Ala Glu Ala 35 40 45 Ala Asp Ala Glu Ala Gly Ala Ala Ala Pro Arg Pro Leu Pro Arg Leu 50 55 60 Arg Pro Pro Ala Cys Ser Leu Val Pro Pro Arg Leu Pro Gln Cys Pro 65 70 75 80 Leu Gln Glu Leu Arg Asn Pro Cys Pro Asp Thr Met Pro Glu Arg Cys 85 90 95 Cys Arg Leu Pro His Met Ile Ala Val Tyr Cys Val 100 105 157 83 PRT Japanese Macaque Herpesvirus 157 Met Arg Ala Arg Pro Asp Gln Asn Ser Pro Pro Pro Ser Gly His Asn 1 5 10 15 Arg Lys Arg Thr Lys His Arg Phe Cys Val Arg Ala Leu Arg Trp Leu 20 25 30 Arg Val Val Glu Arg Ala Ile Tyr Leu Ile Cys Arg Phe Leu His Ala 35 40 45 Val Asn Arg Asp His Val Gly Gln Pro Ala Thr Ser Phe Arg His Ser 50 55 60 Ile Gly Thr Arg Val Ala Lys Phe Leu Gln Gly Thr Leu Arg Lys Thr 65 70 75 80 Arg Arg His 158 86 PRT Japanese Macaque Herpesvirus 158 Met Ala Leu Arg Val Gly Gly Asn Leu Phe Glu Lys Asp Leu Leu Pro 1 5 10 15 Pro Gly Val Lys His Arg His Arg Pro Cys Val Phe Asn His Val Gly 20 25 30 Arg Asn Tyr Ile Asn Ala Ala Ala Gly Asp Ala Arg His Gly Ser Val 35 40 45 Arg Ser Ser Asn Ala Leu Cys Gly Gly Pro Arg Ala Leu Tyr Arg Val 50 55 60 Pro Trp Val Arg Val Asn Asn Ser Pro Gln Arg Ser Tyr Arg Tyr Leu 65 70 75 80 Ala Lys Thr Gly Ile Ala 85 159 253 PRT Japanese Macaque Herpesvirus 159 Met Leu Gly Gly Ile Thr Leu Thr Leu Leu Leu Ala Thr Leu Ala Thr 1 5 10 15 Val Arg Cys Ala Leu Gln Thr His Tyr Ala Ala Val Pro Val His Ser 20 25 30 Thr Ala Ser Leu Gly Cys Val Leu Thr Thr Ala His Asn Val Leu Ile 35 40 45 Val Thr Trp Gln Lys Gln Glu Ser Pro Ser Pro Val Asn Val Ala Thr 50 55 60 Tyr Ser Ser Glu Ala Gly Thr Val Val Gln Pro Pro Phe Ala Gly Arg 65 70 75 80 Val Asp Ile Pro Glu His Lys Leu Thr Arg Thr Thr Leu Lys Phe Phe 85 90 95 Asn Ala Thr Met Glu Asp Glu Gly Cys Tyr Leu Cys Ile Phe Asn Ala 100 105 110 Phe Gly Val Gly Lys Leu Ser Gly Thr Ala Cys Leu Thr Val Tyr Val 115 120 125 Pro Leu Ser Met Ser Val Thr Phe Tyr Pro Pro Ile Asn Pro Thr Gln 130 135 140 Leu Val Cys Arg Ala Glu Ala Ser Pro Ala Pro Ser Val Asn Trp Thr 145 150 155 160 Gly Val Pro Pro Glu Leu Cys Ser Glu Pro Glu Val Phe Pro Arg Pro 165 170 175 Asn Gly Thr Thr Leu Val Val Gly Arg Cys Asn Val Thr Ser Val Asp 180 185 190 Pro Glu Asp Leu Arg Asn Ala Thr Cys Leu Val Thr His Ile Gly Gly 195 200 205 Leu Ala Ser Ala Arg Pro Leu Gly Pro Val Phe Ser Asp Pro Leu Glu 210 215 220 Gly Thr Ser His Tyr Val Val Gly Val Val Ala Ala Val Ala Val Leu 225 230 235 240 Gly Ile Phe Leu Thr Gly Val Phe Leu Tyr Arg Ser Met 245 250 160 165 PRT Japanese Macaque Herpesvirus 160 Met Ser Asp Gln Ala Arg Gly Val Ser Glu Val Phe Gly Ile His Arg 1 5 10 15 Arg Tyr Val Ala Ala Thr His Asp Gln Gly Cys Ser Val Gly Ser Gly 20 25 30 Lys His Phe Gly Phe Ala Ala Gln Leu Gly Trp His Ala Gly Pro Val 35 40 45 Asn Arg Arg Cys Gly Thr Gly Leu Gly Pro Thr Asp Lys Leu Arg Arg 50 55 60 Val Asn Trp Gly Val Lys Arg Asp Gly His Gly Gln Gly Asp Val Asn 65 70 75 80 Arg Gln Ala Gly Gly Ser Arg Gln Leu Ser His Ser Lys Arg Val Lys 85 90 95 Asp Thr Gln Val Ala Pro Leu Val Leu His Ser Gly Ile Lys Lys Leu 100 105 110 Gln Gly Cys Ser Gly Gln Leu Val Phe Gly Asp Val Asn Pro Thr Gly 115 120 125 Glu Arg Gly Leu Asn His Arg Ala Arg Phe Gly Thr Ile Cys Gly His 130 135 140 Val Asn Gly Ala Arg Arg Phe Leu Phe Leu Pro Gly Asn Asp Lys Asn 145 150 155 160 Val Val Gly Cys Cys 165 161 342 PRT Japanese Macaque Herpesvirus 161 Met Asp Ala Leu Asn Asn Asn Leu Asn Leu Leu Met Asp Phe Leu Ser 1 5 10 15 Asn Tyr Ser Asn Ser Tyr Ser Ser Tyr Asp Asp Asn Ile Ser Tyr Thr 20 25 30 Leu Asp Thr Glu Ser Thr Leu Cys Arg Leu Thr Ile Ile Phe Pro Pro 35 40 45 Thr Ile Tyr Ala Ile Ile Cys Phe Phe Ile Phe Cys Ile Thr Leu Leu 50 55 60 Gly Asn Ala Leu Val Leu Tyr Ile Phe Phe Lys Phe Lys Ala Leu Ala 65 70 75 80 Asn Ser Val Asp Val Leu Met Ala Gly Leu Cys Cys Asn Ser Leu Phe 85 90 95 Leu Cys Ala Ser Phe Leu Phe Ser Trp Leu Leu Tyr Val Ala Pro Gln 100 105 110 Ile Leu Thr Pro Ala Thr Cys Lys Val Glu Ile Phe Phe Phe Tyr Leu 115 120 125 Tyr Thr Tyr Phe Gly Val Tyr Ile Val Val Cys Ile Ser Leu Ile Arg 130 135 140 Cys Leu Leu Val Val Phe Ser Arg Arg Pro Trp Val Lys His Trp Ala 145 150 155 160 Ser Gly Phe Leu Cys Val Cys Val Ser Leu Ile Val Ala Leu Ala Leu 165 170 175 Ser Ala Asn Ala Ser Leu Tyr Arg Thr Ala Leu Arg His Pro Glu Thr 180 185 190 Ser Glu Trp Ile Cys Tyr Glu Asp Ala Gly Glu Asp Thr Val Asn Trp 195 200 205 Lys Leu Arg Ile Arg Thr Ile Ser Ala Ile Cys Gly Phe Leu Val Pro 210 215 220 Phe Gly Leu Leu Val Leu Phe Tyr Gly Leu Thr Trp Cys Ile Val Lys 225 230 235 240 Ser Thr Lys Leu Ala Arg Lys Gly Ala Val Arg Gly Val Ile Val Thr 245 250 255 Val Val Val Leu Phe Leu Ile Phe Cys Leu Pro Tyr His Leu Cys Asn 260 265 270 Phe Phe Asp Thr Leu Leu Arg Thr Gly Phe Val Thr Glu Thr Cys Tyr 275 280 285 Ile Arg Asp Val Ile Ser Val Ala Met His Ile Cys Ser Leu Leu Gln 290 295 300 Ser Met Tyr Ser Ala Phe Val Pro Val Val Tyr Ser Gly Leu Gly Ser 305 310 315 320 Leu Phe Arg Arg Arg Val Arg Asp Thr Trp Ser Met Phe Arg Cys Phe 325 330 335 Ser Thr Ser Gly Ser Leu 340 162 1298 PRT Japanese Macaque Herpesvirus 162 Met Ala Gln Arg Thr Asn Pro Arg Trp Ala Ala Ala Ala Leu Ser Ala 1 5 10 15 Asp Glu Glu Ala Phe Ile His Asp Asn Ser Asp Ala Glu Ser Val Leu 20 25 30 Ala Leu Val Pro Glu Gln Cys Phe Ser Glu Phe Leu Leu Trp Leu Val 35 40 45 Thr Arg Pro Ser Asp Asn Phe Asp Asn Asp Asp Asp Asp Pro Thr Leu 50 55 60 Gly Val Ile Trp Gln Leu Leu Ala Pro Leu Val Asn Tyr Ala Pro Leu 65 70 75 80 Glu Thr Arg Ser Ala His Leu Gln Gly His His Thr Ile Ser Leu Pro 85 90 95 Tyr Gly Pro Asp Leu Leu Arg Gln Pro Thr Thr Arg Ser Ser Glu Leu 100 105 110 Val Gln Cys Leu Arg Asp Ser Gly Phe Asp Thr Ala Leu Arg Leu Glu 115 120 125 Leu Ala Arg His Leu Ser Cys Gln Thr Arg Arg Phe Val Ala Asp Arg 130 135 140 Val Pro Pro Gly Thr Phe Ala Ala Leu Thr Leu Gly Ala Leu Val Glu 145 150 155 160 Tyr Asp Val Arg Val Gln Arg Gln Leu Pro Val Thr Val Gln Ser Thr 165 170 175 Ala Trp Arg Pro Leu Pro Glu Arg Asp Pro Ile Cys Ala Ala Val Met 180 185 190 Leu Pro Leu Gln Arg Asn Ile Leu Pro Leu Ala Val Gln Ala Ser Asn 195 200 205 Gly Asn Ser Tyr Thr Val Ser Arg Tyr Ala Val Met Ala Arg Arg Ser 210 215 220 Tyr Gly Cys Val Phe Gln Arg Leu Pro Cys Glu Asn Val Thr His Ile 225 230 235 240 Ala Asp Ser Phe Thr His Leu His Ser Ala Ile Arg Thr Gly Ala Gly 245 250 255 Ala Leu Gln Asp Ile Leu Phe His Ser Thr Leu Leu Pro Gly Gly Asp 260 265 270 Ile Arg Ser Ala Leu Cys Gly Phe Tyr Ala Thr Thr Pro Ser Val Gly 275 280 285 Ala Phe Ser Arg Ala Arg His Arg Ala Ile Asn Thr Thr Thr Thr Leu 290 295 300 His Cys Gln Gln Leu Ala Arg Thr Gly Thr Pro Val Leu Gly Gly Phe 305 310 315 320 Leu Lys Thr Val His Ser Ala Thr Thr Ser Glu Ala Asn Val Ile Thr 325 330 335 Thr Thr Ser Leu Leu Ser Cys Val Pro Gln Ala Tyr Thr Phe Leu Arg 340 345 350 Arg Ser Leu Phe Asn Gln Pro Ile Ile Cys Leu Gly Ser Phe Glu Pro 355 360 365 Val Asp Gly Asp Gly Asn Gln Arg Ser Leu Tyr Leu Gly Ser Ala Ala 370 375 380 Gly Ile Asn Arg Ile Asn Gln Thr Leu Ser Leu Ala Tyr Glu Ile Leu 385 390 395 400 Glu Gly Pro Leu Phe Thr Ser Ile Asn Arg Ala His Glu Pro Ala Ser 405 410 415 Thr Ile Ser His Leu Gly Ala Leu Val Ser Arg Gly Gly Leu Arg Leu 420 425 430 Phe Val Ser Gln Leu Pro Pro Thr Ile Leu Ser Gln Leu Thr Ala Thr 435 440 445 Pro Asp Ile Ser Arg Glu Thr Val Asn Asp Ile Leu Leu Asn Lys Phe 450 455 460 Leu Asn Val Ser Ala Phe Val Val Phe Ala Val Leu Pro Arg Asp Thr 465 470 475 480 Glu Pro Glu Pro Gly Pro Leu Asp Ala Ile Arg Arg Ala Ala Arg Ile 485 490 495 Cys Gly Cys Pro Phe Ala Val Val Gly Glu Thr Cys Glu Glu Pro Gly 500 505 510 Ile Gln Phe Val Asn Asp Leu Glu Leu Trp Asn Pro Gly Ala Trp Pro 515 520 525 Ile Arg Gln Pro Thr Ser Ala Glu Val Ile Ala Thr Phe Gly Phe Asp 530 535 540 Glu Gln Pro Val Ser Ser Asn Trp Leu Val Arg Pro Glu Glu Pro Glu 545 550 555 560 Glu Gly Gly Glu Gln Ala Pro Ser Pro Thr Asp Trp Gly Leu Phe Arg 565 570 575 Leu Ala Ser Val Val Asp Gln Leu Leu Arg Cys Pro Thr Val Gly Ser 580 585 590 Lys Glu Phe Val Thr Arg His Val Asp Arg Cys Ser Asn Gly Leu Val 595 600 605 Ala Gln Gln Cys Glu Val Gly Pro Leu Gly Arg Pro Leu Ser Asp Tyr 610 615 620 His Ile Val Asn His Thr Ala Val Phe Thr Asp Arg Met Ala Arg Val 625 630 635 640 Pro Ile His Arg Pro Gln Pro Ile Thr Arg Gln Asp Ala Thr Glu Arg 645 650 655 Leu Gly Ser Pro Glu Thr Trp Val Thr Gln Gly Arg Gly Arg Leu Arg 660 665 670 Trp Val Gly Gln Cys Val Ala His Gly Glu Gln Ala Tyr Lys Met Gly 675 680 685 Ile Asp Ala Ala Val Gly Ala Arg Tyr Ala Ile Cys Glu Ala Val Thr 690 695 700 Asn Ile Met Leu Ala His Val Arg Arg Leu Ser Asp Ile Thr Leu Thr 705 710 715 720 Ala Ser Val Gly Trp Asn Pro Glu Glu Asp Gln Ala Trp Leu Leu Gln 725 730 735 His Ala Leu Phe Ala Cys Lys Glu Leu Cys Arg Asp Leu Ser Val Asn 740 745 750 Phe Ala Ile Thr Ser Ala Gly Ser Thr Pro Cys Leu Ser Glu Glu Leu 755 760 765 Ile Ser Ala Thr Gln Gln His Gln Thr Val Ala Pro Val Pro Phe Asn 770 775 780 Ala Val Ile Ile Thr Ala Thr Ala Glu Val Lys Ser Ser Arg Arg Arg 785 790 795 800 Val Thr Pro Asp Leu Lys Ala Thr Gly Asn Leu Leu Val Leu Val Thr 805 810 815 Phe Pro Gly Pro His Leu Thr Gln Gly Ser Thr Phe Glu His Leu Cys 820 825 830 Leu Leu Pro Ser Pro Thr Leu Pro Asp Val Gln Ala Thr His Leu Ala 835 840 845 Asn Leu Phe Met Leu Thr Glu Ser Met Leu Ser Arg Gly Leu Val Val 850 855 860 Ser Gly His Asp Val Ser Asp Gly Gly Val Val Val Thr Ala Ile Glu 865 870 875 880 Met Ala Leu Ala Gly Asn Arg Gly Leu Gln Ile Cys Ile Pro Ser Glu 885 890 895 Glu Thr Pro Leu Pro Trp Leu Val Ser Glu Thr Pro Gly Val Ile Phe 900 905 910 Glu Ile Leu Pro Gln His Val Asp Glu Val Arg Gln Ala Cys Gln Asn 915 920 925 Phe Asp Cys Gln Ala Thr Val Cys Gly Thr Val Gly Gln Glu Gly Leu 930 935 940 Ser Glu Arg Ile Val Ile Ser His Asn Asn Glu Glu Val Tyr Ser Gln 945 950 955 960 Thr Leu Thr Ser Val Ala Ala Asn Trp Thr Ser Phe Ser Asp Glu Gln 965 970 975 Trp Tyr Ser Trp Gly Pro Ser Phe Thr Pro Ala Gln Glu Leu Tyr Arg 980 985 990 Lys Asp Tyr Gly Cys Asn Arg His Asn Leu Gly His Leu Ala Asp Val 995 1000 1005 Cys Arg Asn Ser Glu Leu Thr Leu Phe Ala Val Pro Ser Arg Pro 1010 1015 1020 Pro Ala Val Ala Ala Leu Ile Ala Pro Gly Ala Pro Leu Pro Arg 1025 1030 1035 Ala Leu Met Ala Ala Phe Thr Asn Val Gly Phe Asp Val Ala Ala 1040 1045 1050 Val Ser Thr Asn Asp Leu Arg Gly Gly Asn Ile Leu Arg Gly Phe 1055 1060 1065 Ser Gly Leu Thr Ile Gly Gly Asn Val Gly Ile Glu Asp Ser Tyr 1070 1075 1080 Val Gly Ala Arg Cys Ala Ile Met Gly Leu Leu Asn Asp Pro Gly 1085 1090 1095 Cys Tyr Gly Gly Leu Met Ala Phe Phe Arg Arg Ala Asp Thr Phe 1100 1105 1110 Ser Leu Cys Cys Gly Glu Phe Gly Phe Gln Leu Leu Gly Ala Leu 1115 1120 1125 Gly Leu Leu Arg Glu Thr Pro His Asp Thr Pro Gly Pro Lys Thr 1130 1135 1140 Pro Asp Gln Trp Asp Ile His Leu Glu Glu Asn Ala Ser Gly Asn 1145 1150 1155 His Glu Cys Leu Trp Leu Asn Leu His Ile Pro Gln Thr Thr Ile 1160 1165 1170 Ser Ile Met Phe Arg Val Leu Arg Gly Leu Val Leu Pro Gly Trp 1175 1180 1185 Ala Asn Gly Arg Tyr Leu Gly Val Arg Tyr Pro Arg Asp Ala Ile 1190 1195 1200 Glu Tyr His Leu Asn Gln Gln Gln Arg Ile Ala Leu Asn Phe His 1205 1210 1215 Thr Gly Asn Pro Asp Pro Arg Met Phe Ala Gln His Tyr Pro Arg 1220 1225 1230 Asn Pro Ser Ala Asn Ser Ala Val Ala Ala Ile Thr Ser Pro Asp 1235 1240 1245 Gly Arg His Leu Ala Ser Leu Val Asp Pro Ala Val Val Phe His 1250 1255 1260 Pro Trp Gln Trp Ala Tyr Val Pro Pro Glu Leu Ala Asp Met Thr 1265 1270 1275 Ile Ser Pro Trp Ala Leu Ala Phe Gln Ser Leu Phe Leu Trp Cys 1280 1285 1290 Val Arg Asn Arg Gln 1295 163 90 PRT Japanese Macaque Herpesvirus 163 Met Arg Asn His Gly Ser Ser Gln Arg Pro Trp Val Leu Trp Gly Pro 1 5 10 15 Tyr Gly Ile Leu Pro Pro Ser Gly Tyr Ile Phe Thr Val Leu Arg Gly 20 25 30 Val Trp Val Pro Ala Pro Gly Gly Ala Arg Ser Thr Gln Arg Asn Pro 35 40 45 Ser Arg His Ala Arg Ala Gln Asn Pro Arg Pro Val Gly His Pro Pro 50 55 60 Gly Gly Glu Arg Ile Arg Glu Pro Arg Val Pro Leu Ala Lys Pro Pro 65 70 75 80 His Pro Pro Asp His His Gln His Asn Val 85 90 164 84 PRT Japanese Macaque Herpesvirus 164 Met Pro Thr Phe Pro Pro Met Val Lys Pro Glu Asn Pro Arg Arg Met 1 5 10 15 Phe Pro Pro Leu Arg Ser Leu Val Glu Thr Ala Ala Thr Ser Asn Pro 20 25 30 Thr Leu Val Asn Ala Ala Ile Ser Ala Leu Gly Ser Gly Ala Pro Gly 35 40 45 Ala Ile Arg Ala Ala Thr Ala Gly Gly Leu Asp Gly Thr Ala Asn Ser 50 55 60 Val Ser Ser Leu Phe Leu Gln Thr Ser Ala Arg Trp Pro Arg Leu Cys 65 70 75 80 Arg Leu His Pro 165 107 PRT Japanese Macaque Herpesvirus 165 Met Thr Ile Leu Ser Asp Arg Pro Ser Trp Pro Thr Val Pro His Thr 1 5 10 15 Val Ala Trp Gln Ser Lys Phe Trp His Ala Trp Arg Thr Ser Ser Thr 20 25 30 Cys Trp Gly Arg Ile Ser Lys Ile Thr Pro Gly Val Ser Asp Thr Ser 35 40 45 His Gly Arg Gly Val Ser Ser Asp Gly Met Gln Ile Cys Arg Pro Arg 50 55 60 Leu Pro Ala Arg Ala Ile Ser Ile Ala Val Thr Thr Thr Pro Pro Ser 65 70 75 80 Leu Thr Ser Trp Pro Asp Thr Thr Arg Pro Arg Glu Ser Ile Asp Ser 85 90 95 Val Ser Ile Lys Arg Leu Ala Arg Cys Val Ala 100 105 166 131 PRT Japanese Macaque Herpesvirus 166 Met Ala Lys Phe Thr Leu Arg Ser Arg His Ser Ser Leu Gln Ala Asn 1 5 10 15 Ser Ala Cys Cys Ser Ser Gln Ala Trp Ser Ser Ser Gly Phe Gln Pro 20 25 30 Thr Asp Ala Val Ser Val Met Ser Leu Arg Arg Arg Thr Cys Ala Ser 35 40 45 Met Met Leu Val Thr Ala Ser Gln Met Ala Tyr Leu Ala Pro Thr Ala 50 55 60 Ala Ser Met Pro Ile Leu Tyr Ala Cys Ser Pro Trp Ala Thr His Cys 65 70 75 80 Pro Thr His Leu Ser Leu Pro Leu Pro Trp Val Thr Gln Val Ser Gly 85 90 95 Leu Pro Arg Arg Ser Val Ala Ser Cys Leu Val Ile Gly Trp Gly Arg 100 105 110 Cys Met Gly Thr Arg Ala Ile Leu Ser Val Asn Thr Ala Val Trp Leu 115 120 125 Thr Met Trp 130 167 160 PRT Japanese Macaque Herpesvirus 167 Met Pro Phe Cys Arg Arg Arg Gly Asn Leu Arg Arg Ala Gly Asn Pro 1 5 10 15 Val Arg Glu Arg Pro Arg Ala Val Glu Pro Gly Ser Val Ala Asp Gln 20 25 30 Thr Ala Asp Leu Gly Arg Ser Asp Arg Asn Phe Trp Val Arg Arg Ala 35 40 45 Ala Arg Phe Leu Gln Leu Ala Gly Ala Pro Arg Arg Thr Gly Gly Gly 50 55 60 Arg Arg Thr Gly Thr Leu Ala Asp Arg Leu Gly Pro Ile Pro Pro Gly 65 70 75 80 Leu Arg Gly Arg Ser Ala Ser Ala Met Ser Asn Arg Arg Gln Gln Arg 85 90 95 Val Cys His Ala Thr Cys Gly Gln Met Leu Gln Arg Thr Arg Ser Ser 100 105 110 Ala Val Arg Ser Gly Thr Pro Gly Pro Thr Ala Val Arg Leu Pro His 115 120 125 Arg Gln Pro His Gly Gly Val Tyr Gly Gln Asn Gly Ala Gly Ala His 130 135 140 Thr Ser Pro Pro Thr Asp His Gln Ala Gly Arg Asp Gly Thr Pro Gly 145 150 155 160 168 102 PRT Japanese Macaque Herpesvirus 168 Met Phe Arg Cys Asn Gly Ser Ile Thr Ala Ala His Ile Gly Ser Leu 1 5 10 15 Ser Gly Asn Gly Leu Gln Ala Val Asp Cys Thr Val Thr Gly Ser Trp 20 25 30 Arg Cys Thr Arg Thr Ser Tyr Ser Thr Ser Ala Pro Ser Val Arg Ala 35 40 45 Ala Asn Val Pro Gly Gly Thr Arg Ser Ala Thr Asn Arg Leu Val Trp 50 55 60 Gln Leu Arg Cys Leu Ala Ser Ser Asn Arg Asn Ala Val Ser Lys Pro 65 70 75 80 Leu Ser Leu Arg His Cys Thr Ser Ser Leu Asp Leu Val Val Gly Trp 85 90 95 Arg Ser Arg Ser Gly Pro 100 169 123 PRT Japanese Macaque Herpesvirus 169 Met Phe Val Ser Phe Ala Thr Met Gly Asn Thr Tyr Asp Phe Tyr Asn 1 5 10 15 Asn Asn Ile Met Glu Trp Thr Leu Gln Asn Tyr Thr Leu Asn Thr Ala 20 25 30 Asn Ile Tyr Ser Asn Gly Ile Leu Trp Ile Cys Met Val Lys Phe Thr 35 40 45 Asn Lys His Cys Lys Asn Asn Trp Ile Val Val Cys Asn Ile Cys Arg 50 55 60 Tyr Val Ala Ile Leu Leu Leu Phe Ile Ile Asn Arg Gly Asn Ile Tyr 65 70 75 80 Glu Glu Ile Asn Cys Leu Phe Phe Val Thr Ala Leu Ile Gly Met Tyr 85 90 95 Ala Val Thr Glu Ala Ser Thr Thr Ser Ser Leu Thr Met Ala Leu Ala 100 105 110 Tyr Ser Ile Ile Thr Ala Asn Thr Gly Ile Phe 115 120 170 85 PRT Japanese Macaque Herpesvirus 170 Met Ala Cys Asn Cys Pro Phe Phe Val Trp Cys Thr Trp Leu Phe Ser 1 5 10 15 Asn Ile Leu Thr Gly Thr Phe Trp Leu Ile Ser Leu Ala Gln Tyr Ala 20 25 30 Cys Asp Asn Asn Lys Asp Leu Tyr Ile Val Ala Val Ser Thr Val Ala 35 40 45 Cys Phe Phe Phe Leu Trp Lys Ser Leu Gly Leu Tyr Phe Tyr Gln Ser 50 55 60 Arg Ser Gln Arg Leu Asn Thr Pro Leu Leu Lys Leu Ile Pro Trp Ile 65 70 75 80 Thr Gly Met Thr Leu 85 171 144 PRT Japanese Macaque Herpesvirus 171 Met Pro Gly Gly Gly Arg Pro Ala Ser Gly Ala Ala Arg Arg Gly Leu 1 5 10 15 Trp Gly Pro Gly Leu Gly Gly Arg Arg Gly Ala Ala Pro Pro Gly Ser 20 25 30 Ala Gly Pro Gly Arg Ser Arg Glu Ser Ala Gly Pro Gly Gly Ala Gly 35 40 45 Pro Gly Gly Gly Pro Gly Pro Pro Arg Asp Pro Arg Pro Arg Glu Pro 50 55 60 Lys Ala Ala Arg Arg Ala Ala Arg Gly Gly Arg Gly Arg Arg Pro Arg 65 70 75 80 Ala Arg Ala Gly Arg Ala Glu Gly Arg Glu Pro Gly Glu Ala Gly Gly 85 90 95 Ala Pro Leu Gly Gly Pro Gly Ala Ala Arg Glu Thr Leu Ala Pro Gly 100 105 110 Ala Arg Trp Arg Pro Arg Pro Arg Ala Ala Ala Gly Arg Ala Pro Gly 115 120 125 Gly Pro Arg Arg Ala Pro Pro Leu Gly Ala Leu Ala Trp Arg Arg Cys 130 135 140 172 91 PRT Japanese Macaque Herpesvirus 172 Met Pro Gly Gly Arg Arg Pro Ala Trp Arg Ser Ser Ala Gly Leu Pro 1 5 10 15 Ser Pro Thr Ser Pro Arg Lys Val Val Ser Ala Pro Pro Gly Gly Gly 20 25 30 Leu Gly Pro Gly Ala Pro Arg Arg Gly Arg Pro Arg Gly Ala Thr Glu 35 40 45 Gly Pro Gly Arg Thr Gly Asp Arg Glu Asn Ala Arg Gly Gly Gly Gly 50 55 60 Gln Arg Gly Thr Cys Ala Cys Leu Trp Asn Thr Met Ala Cys Trp Pro 65 70 75 80 Ala Arg Leu Leu Gly Ser Leu Gln Ala Cys Cys 85 90 

1. An isolated viral nucleic acid comprising a nucleic acid sequence at least 90% identical to the nucleic acid sequence set forth as SEQ ID NO:
 1. 2. A host cell transformed with the virus of claim
 1. 3. A polypeptide at least 95% identical to a polypeptide encoded by the nucleic acid of SEQ ID NO:
 1. 4. The polypeptide of claim 3, wherein the polypeptide is 100% identical to the polypeptide encoded by SEQ ID NO:
 1. 5. The polypeptide of claim 3, wherein the polypeptide encoded by nucleic acid 21845 to nucleic acid 22120 of SEQ ID NO: 1 (JMHV25), nucleic acid 22363 to nucleic acid 22701 of SEQ ID NO: 1 (JMHV26), nucleic acid 33254 to nucleic acid 33553 of SEQ ID NO: 1 (JMHV39), nucleic acid 35301 to nucleic acid 35687 of SEQ ID NO: 1 (JMVH41), nucleic acid 40188 to nucleic acid 40439 of SEQ ID NO: 1 (JMHV48), nucleic acid 45836 to nucleic acid 46195 of SEQ ID NO: 1 (JMHV54), nucleic acid 47768 to nucleic acid 48136 of SEQ ID NO: 1 (JM57), nucleic acid 57325 to nucleic acid 57573 of SEQ ID NO: 1 (JM71), nucleic acid 62823 to nucleic acid 63086 of SEQ ID NO: 1 (JM76), nucleic acid 65629 to nucleic acid 65880 of SEQ ID NO: 1 (JM80), nucleic acid 67920 to nucleic acid 68594 of SEQ ID NO: 1 (JM85), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM87) nucleic acid 70328 to nucleic acid 70606 of SEQ ID NO: 1 (JM88), nucleic acid 75447 to nucleic acid 75722 of SEQ ID NO: 1 (JM95), nucleic acid 105581 to nucleic acid 106003 of SEQ ID NO: 1 (JM132), nucleic acid 117501 to nucleic acid 118265 of SEQ ID NO: 1 (JM152), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM159), nucleic acid to nucleic acid of SEQ ID NO: 1 (JM166), and nucleic acid to nucleic acid of SEQ ID NO: 1 (JM167).
 6. The polypeptide of claim 5, wherein the polypeptide comprises an amino acid sequence set forth as one of SEQ ID NOs: 1-171.
 7. An antibody that specifically binds the polypeptide of claim
 3. 8. The antibody of claim 7, wherein the antibody is a monoclonal antibody.
 9. A nucleic acid encoding the polypeptide of claim
 3. 10. The nucleic acid of claim 9, operably linked to a promoter.
 11. A vector comprising the nucleic acid of claim
 10. 12. The vector of claim 11, wherein the vector is a viral vector.
 13. A method for testing the efficacy of an agent for the treatment a symptom associated with multiple sclerosis, the method comprising: (a) administering the agent to a non-human primate infected with a virus comprising the nucleic acid sequence of claim 1; and (b) observing the non-human primate to determine if the drug inhibits the presentation of one or more symptoms associated with Japanese macaque herpesvirus (JMHV) infection as compared to a non-human primate not administered the agent.
 14. The method of claim 13, wherein the agent is a drug used to treat multiple sclerosis.
 15. The method of claim 13, wherein the non-human primate is a Japanese macaque monkey.
 16. The method of claim 13, wherein the symptom is associated with multiple sclerosis.
 17. A method of detecting the presence of a virus in a biological specimen, comprising: (a) amplifying by polymerase chain reaction a Japanese macaque herpesvirus (JMHV) nucleic acid sequence, if such sequence is present in the sample, using two or more oligonucleotide primers comprising 20 contiguous nucleotides of the nucleic acid sequence of claim 1 to form an amplified sequence; and (b) determining whether an amplified sequence is present.
 18. The method of claim 17, wherein the step of determining whether an amplified sequence is present comprises one or more of: (a) electrophoresis and staining of the amplified sequence; or (b) hybridization the amplified sequence to a probe.
 19. The method of claim 18, wherein the probe comprises a detectable non-isotopic label comprising a fluorescent molecule, a chemiluminescent molecule, an enzyme, a co-factor, an enzyme substrate; or a hapten.
 20. The method of claim 17, wherein the biological specimen is a non-human primate specimen.
 21. A method of detecting the presence of Japanese macaque herpesvirus (JMHV) in a biological specimen, comprising: (a) exposing the biological specimen to a probe that hybridizes to a Japanese macaque herpesvirus (JMHV) nucleic acid sequence of claim 1, if the sequence is present in the sample to form a hybridization complex; and (b) determining whether the hybridization complex is present, thereby detecting the presence of the Japanese macaque herpesvirus (JMHV).
 22. The method of claim 21, wherein the primate specimen is a non-human primate specimen.
 23. A method of detecting the presence of Japanese macaque herpesvirus (JMHV) in a biological specimen, comprising: (a) contacting the biological specimen with the antibody of claim 5, (b) detecting binding of the antibody to the biological specimen or a component thereof, wherein binding of the antibody to the biological specimen indicates the presence of a Japanese macaque herpesvirus (JMHV).
 24. The method of claim 23, wherein the antibody comprises a detectable label.
 25. The method of claim 24, wherein the detectable label comprises a fluorescent molecule, a chemiluminescent molecule, an enzyme, a co-factor, an enzyme substrate; or a hapten.
 26. A kit comprising a container means comprising an oligonucleotide primer comprising at least 15 contiguous nucleotides of the nucleic acid sequence of claim
 1. 27. A kit comprising a container means comprising an antibody of claim
 7. 28. A non-human primate model for multiple sclerosis, comprising a non-human primate infected with a virus comprising the nucleic acid sequence of claim 1, wherein the non-human primate exhibits a symptom or a pathological feature of multiple sclerosis.
 29. The non-human primate model of claim 28, wherein the symptom is acute onset paresis or paralysis involving one or more limbs.
 30. The non-human primate model of claim 28, wherein the pathological feature is myelin destruction in a central nervous system.
 31. The non-human primate model of claim 28, wherein the non-human primate is a Japanese macaque.
 32. An isolated virus comprising the nucleic acid of claim
 1. 